Canonical Allele Identifier: CA1978884887
Gene: MEN1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64804745_64804760delinsTTCCTCGCCCCACGGC , CM000673.2:g.64804745_64804760delinsTTCCTCGCCCCACGGC GRCh38
NC_000011.9:g.64572217_64572232delinsTTCCTCGCCCCACGGC , CM000673.1:g.64572217_64572232delinsTTCCTCGCCCCACGGC GRCh37
NC_000011.8:g.64328793_64328808delinsTTCCTCGCCCCACGGC NCBI36
NG_008929.1:g.11535_11550delinsGCCGTGGGGCGAGGAA , LRG_509:g.11535_11550delinsGCCGTGGGGCGAGGAA
NG_033040.1:g.3482_3497delinsGCCGTGGGGCGAGGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000377313.7:c.1422_1437delinsGCCGTGGGGCGAGGAA ENSP00000366530.1:p.Glu474=
ENST00000394374.8:c.*715_*730delinsGCCGTGGGGCGAGGAA ENSP00000377899.4:n.*715_*730delinsGCCGTGGGGCGAGGAA
ENST00000394376.7:c.1398_1413delinsGCCGTGGGGCGAGGAA ENSP00000377901.3:p.Glu466=
ENST00000413626.2:c.1407_1422delinsGCCGTGGGGCGAGGAA ENSP00000411218.2:p.Glu469=
ENST00000424912.2:c.1407_1422delinsGCCGTGGGGCGAGGAA ENSP00000388016.2:p.Glu469=
ENST00000429702.6:c.1407_1422delinsGCCGTGGGGCGAGGAA ENSP00000402752.2:p.Glu469=
ENST00000672079.2:c.*503_*518delinsGCCGTGGGGCGAGGAA ENSP00000500905.2:n.*503_*518delinsGCCGTGGGGCGAGGAA
ENST00000710881.1:c.1422_1437delinsGCCGTGGGGCGAGGAA ENSP00000518530.1:p.Glu474=
ENST00000394374.7:c.1154_1169delinsGCCGTGGGGCGAGGAA
ENST00000394376.6:c.749_764delinsGCCGTGGGGCGAGGAA
ENST00000478548.3:n.1900_1915delinsGCCGTGGGGCGAGGAA
ENST00000671939.2:n.1369_1384delinsGCCGTGGGGCGAGGAA
ENST00000671965.2:n.1789_1804delinsGCCGTGGGGCGAGGAA
ENST00000312049.11:c.1407_1422delinsGCCGTGGGGCGAGGAA ENSP00000308975.6:p.Glu469=
ENST00000315422.9:c.1407_1422delinsGCCGTGGGGCGAGGAA ENSP00000323747.4:p.Glu469=
ENST00000377313.6:c.1422_1437delinsGCCGTGGGGCGAGGAA ENSP00000366530.1:p.Glu474=
ENST00000440873.6:c.1407_1422delinsGCCGTGGGGCGAGGAA ENSP00000413944.2:p.Glu469=
ENST00000450708.7:c.1407_1422delinsGCCGTGGGGCGAGGAA MANE Select ENSP00000394933.3:p.Glu469=
ENST00000478548.2:n.1908_1923delinsGCCGTGGGGCGAGGAA
ENST00000671939.1:n.1684_1699delinsGCCGTGGGGCGAGGAA
ENST00000672304.1:c.1533_1548delinsGCCGTGGGGCGAGGAA ENSP00000500585.1:p.Glu511=
ENST00000312049.10:c.1407_1422delinsGCCGTGGGGCGAGGAA ENSP00000308975.6:p.Glu469=
ENST00000315422.8:c.1407_1422delinsGCCGTGGGGCGAGGAA ENSP00000323747.4:p.Glu469=
ENST00000337652.5:c.1422_1437delinsGCCGTGGGGCGAGGAA ENSP00000337088.1:p.Glu474=
ENST00000377313.5:c.1422_1437delinsGCCGTGGGGCGAGGAA ENSP00000366530.1:p.Glu474=
ENST00000377316.6:c.1242_1257delinsGCCGTGGGGCGAGGAA ENSP00000366533.1:p.Glu414=
ENST00000377321.5:c.1302_1317delinsGCCGTGGGGCGAGGAA ENSP00000366538.1:p.Glu434=
ENST00000377326.7:c.1407_1422delinsGCCGTGGGGCGAGGAA ENSP00000366543.3:p.Glu469=
ENST00000394374.6:c.1422_1437delinsGCCGTGGGGCGAGGAA ENSP00000377899.2:p.Glu474=
ENST00000394376.5:c.1422_1437delinsGCCGTGGGGCGAGGAA ENSP00000377901.1:p.Glu474=
ENST00000478548.1:n.956_971delinsGCCGTGGGGCGAGGAA
NM_000244.3:c.1422_1437delinsGCCGTGGGGCGAGGAA , LRG_509t1:c.1422_1437delinsGCCGTGGGGCGAGGAA NP_000235.2:p.Glu474=
NM_130799.2:c.1407_1422delinsGCCGTGGGGCGAGGAA , LRG_509t2:c.1407_1422delinsGCCGTGGGGCGAGGAA NP_570711.1:p.Glu469=
NM_130800.2:c.1422_1437delinsGCCGTGGGGCGAGGAA NP_570712.1:p.Glu474=
NM_130801.2:c.1422_1437delinsGCCGTGGGGCGAGGAA NP_570713.1:p.Glu474=
NM_130802.2:c.1422_1437delinsGCCGTGGGGCGAGGAA NP_570714.1:p.Glu474=
NM_130803.2:c.1422_1437delinsGCCGTGGGGCGAGGAA NP_570715.1:p.Glu474=
NM_130804.2:c.1422_1437delinsGCCGTGGGGCGAGGAA NP_570716.1:p.Glu474=
XM_005274001.3:c.1407_1422delinsGCCGTGGGGCGAGGAA XP_005274058.1:p.Glu469=
XM_011545040.1:c.1533_1548delinsGCCGTGGGGCGAGGAA XP_011543342.1:p.Glu511=
XM_011545041.1:c.1533_1548delinsGCCGTGGGGCGAGGAA XP_011543343.1:p.Glu511=
XM_011545042.1:c.1533_1548delinsGCCGTGGGGCGAGGAA XP_011543344.1:p.Glu511=
XM_005274001.4:c.1407_1422delinsGCCGTGGGGCGAGGAA XP_005274058.1:p.Glu469=
XM_011545041.2:c.1533_1548delinsGCCGTGGGGCGAGGAA XP_011543343.1:p.Glu511=
XM_011545042.3:c.1533_1548delinsGCCGTGGGGCGAGGAA XP_011543344.1:p.Glu511=
XM_017017765.1:c.1548_1563delinsGCCGTGGGGCGAGGAA XP_016873254.1:p.Glu516=
XM_017017766.1:c.1548_1563delinsGCCGTGGGGCGAGGAA XP_016873255.1:p.Glu516=
XM_017017767.2:c.1548_1563delinsGCCGTGGGGCGAGGAA XP_016873256.1:p.Glu516=
XM_017017768.1:c.1548_1563delinsGCCGTGGGGCGAGGAA XP_016873257.1:p.Glu516=
XM_017017769.1:c.1407_1422delinsGCCGTGGGGCGAGGAA XP_016873258.1:p.Glu469=
XM_017017770.2:c.1407_1422delinsGCCGTGGGGCGAGGAA XP_016873259.1:p.Glu469=
NM_001370251.1:c.1533_1548delinsGCCGTGGGGCGAGGAA NP_001357180.1:p.Glu511=
NM_001370259.2:c.1407_1422delinsGCCGTGGGGCGAGGAA MANE Select NP_001357188.2:p.Glu469=
NM_001370260.1:c.1407_1422delinsGCCGTGGGGCGAGGAA NP_001357189.1:p.Glu469=
NM_001370261.1:c.1407_1422delinsGCCGTGGGGCGAGGAA NP_001357190.1:p.Glu469=
NM_001370262.1:c.1302_1317delinsGCCGTGGGGCGAGGAA NP_001357191.1:p.Glu434=
NM_001370263.1:c.1302_1317delinsGCCGTGGGGCGAGGAA NP_001357192.1:p.Glu434=
NM_000244.4:c.1422_1437delinsGCCGTGGGGCGAGGAA NP_000235.3:p.Glu474=
NM_001370251.2:c.1533_1548delinsGCCGTGGGGCGAGGAA NP_001357180.2:p.Glu511=
NM_001370260.2:c.1407_1422delinsGCCGTGGGGCGAGGAA NP_001357189.2:p.Glu469=
NM_001370261.2:c.1407_1422delinsGCCGTGGGGCGAGGAA NP_001357190.2:p.Glu469=
NM_001370262.2:c.1302_1317delinsGCCGTGGGGCGAGGAA NP_001357191.2:p.Glu434=
NM_001370263.2:c.1302_1317delinsGCCGTGGGGCGAGGAA NP_001357192.2:p.Glu434=
NM_130799.3:c.1407_1422delinsGCCGTGGGGCGAGGAA NP_570711.2:p.Glu469=
NM_130800.3:c.1422_1437delinsGCCGTGGGGCGAGGAA NP_570712.2:p.Glu474=
NM_130801.3:c.1422_1437delinsGCCGTGGGGCGAGGAA NP_570713.2:p.Glu474=
NM_130802.3:c.1422_1437delinsGCCGTGGGGCGAGGAA NP_570714.2:p.Glu474=
NM_130803.3:c.1422_1437delinsGCCGTGGGGCGAGGAA NP_570715.2:p.Glu474=
NM_130804.3:c.1422_1437delinsGCCGTGGGGCGAGGAA NP_570716.2:p.Glu474=