Canonical Allele Identifier: CA2499221137
Gene: MEN1 HGNC NCBI

Linked Data

dbSNP Id: rs2136079359

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.64804446_64804468del , CM000673.2:g.64804446_64804468del GRCh38
NC_000011.9:g.64571918_64571940del , CM000673.1:g.64571918_64571940del GRCh37
NC_000011.8:g.64328494_64328516del NCBI36
NG_008929.1:g.11827_11849del , LRG_509:g.11827_11849del
NG_033040.1:g.3774_3796del

Transcript Alleles

HGVS Amino-acid change
ENST00000377313.7:c.1714_1736del ENSP00000366530.1:p.Ala572HisfsTer22
ENST00000394374.8:c.*1007_*1029del ENSP00000377899.4:n.*1007_*1029del
ENST00000394376.7:c.1690_1712del ENSP00000377901.3:p.Ala564HisfsTer22
ENST00000413626.2:c.1699_1721del ENSP00000411218.2:p.Ala567HisfsTer22
ENST00000424912.2:c.1699_1721del ENSP00000388016.2:p.Ala567HisfsTer22
ENST00000429702.6:c.1699_1721del ENSP00000402752.2:p.Ala567HisfsTer22
ENST00000672079.2:c.*795_*817del ENSP00000500905.2:n.*795_*817del
ENST00000710881.1:c.1714_1736del ENSP00000518530.1:p.Ala572HisfsTer22
ENST00000394376.6:c.1041_1063del
ENST00000478548.3:n.2192_2214del
ENST00000671939.2:n.1661_1683del
ENST00000312049.11:c.1699_1721del ENSP00000308975.6:p.Ala567HisfsTer22
ENST00000315422.9:c.1699_1721del ENSP00000323747.4:p.Ala567HisfsTer22
ENST00000377313.6:c.1714_1736del ENSP00000366530.1:p.Ala572HisfsTer22
ENST00000440873.6:c.1699_1721del ENSP00000413944.2:p.Ala567HisfsTer22
ENST00000450708.7:c.1699_1721del MANE Select ENSP00000394933.3:p.Ala567HisfsTer22
ENST00000478548.2:n.2200_2222del
ENST00000671939.1:n.1976_1998del
ENST00000672304.1:c.1825_1847del ENSP00000500585.1:p.Ala609HisfsTer22
ENST00000312049.10:c.1699_1721del ENSP00000308975.6:p.Ala567HisfsTer22
ENST00000315422.8:c.1699_1721del ENSP00000323747.4:p.Ala567HisfsTer22
ENST00000337652.5:c.1714_1736del ENSP00000337088.1:p.Ala572HisfsTer22
ENST00000377313.5:c.1714_1736del ENSP00000366530.1:p.Ala572HisfsTer22
ENST00000377316.6:c.1534_1556del ENSP00000366533.1:p.Ala512HisfsTer22
ENST00000377321.5:c.1594_1616del ENSP00000366538.1:p.Ala532HisfsTer22
ENST00000377326.7:c.1699_1721del ENSP00000366543.3:p.Ala567HisfsTer22
ENST00000394374.6:c.1714_1736del ENSP00000377899.2:p.Ala572HisfsTer22
ENST00000394376.5:c.1714_1736del ENSP00000377901.1:p.Ala572HisfsTer22
ENST00000478548.1:n.1248_1270del
NM_000244.3:c.1714_1736del , LRG_509t1:c.1714_1736del NP_000235.2:p.Ala572HisfsTer22
NM_130799.2:c.1699_1721del , LRG_509t2:c.1699_1721del NP_570711.1:p.Ala567HisfsTer22
NM_130800.2:c.1714_1736del NP_570712.1:p.Ala572HisfsTer22
NM_130801.2:c.1714_1736del NP_570713.1:p.Ala572HisfsTer22
NM_130802.2:c.1714_1736del NP_570714.1:p.Ala572HisfsTer22
NM_130803.2:c.1714_1736del NP_570715.1:p.Ala572HisfsTer22
NM_130804.2:c.1714_1736del NP_570716.1:p.Ala572HisfsTer22
XM_005274001.3:c.1699_1721del XP_005274058.1:p.Ala567HisfsTer22
XM_011545040.1:c.1825_1847del XP_011543342.1:p.Ala609HisfsTer22
XM_011545041.1:c.1825_1847del XP_011543343.1:p.Ala609HisfsTer22
XM_011545042.1:c.1825_1847del XP_011543344.1:p.Ala609HisfsTer22
XM_005274001.4:c.1699_1721del XP_005274058.1:p.Ala567HisfsTer22
XM_011545041.2:c.1825_1847del XP_011543343.1:p.Ala609HisfsTer22
XM_011545042.3:c.1825_1847del XP_011543344.1:p.Ala609HisfsTer22
XM_017017765.1:c.1840_1862del XP_016873254.1:p.Ala614HisfsTer22
XM_017017766.1:c.1840_1862del XP_016873255.1:p.Ala614HisfsTer22
XM_017017767.2:c.1840_1862del XP_016873256.1:p.Ala614HisfsTer22
XM_017017768.1:c.1840_1862del XP_016873257.1:p.Ala614HisfsTer22
XM_017017769.1:c.1699_1721del XP_016873258.1:p.Ala567HisfsTer22
XM_017017770.2:c.1699_1721del XP_016873259.1:p.Ala567HisfsTer22
NM_001370251.1:c.1825_1847del NP_001357180.1:p.Ala609HisfsTer22
NM_001370259.2:c.1699_1721del MANE Select NP_001357188.2:p.Ala567HisfsTer22
NM_001370260.1:c.1699_1721del NP_001357189.1:p.Ala567HisfsTer22
NM_001370261.1:c.1699_1721del NP_001357190.1:p.Ala567HisfsTer22
NM_001370262.1:c.1594_1616del NP_001357191.1:p.Ala532HisfsTer22
NM_001370263.1:c.1594_1616del NP_001357192.1:p.Ala532HisfsTer22
NM_000244.4:c.1714_1736del NP_000235.3:p.Ala572HisfsTer22
NM_001370251.2:c.1825_1847del NP_001357180.2:p.Ala609HisfsTer22
NM_001370260.2:c.1699_1721del NP_001357189.2:p.Ala567HisfsTer22
NM_001370261.2:c.1699_1721del NP_001357190.2:p.Ala567HisfsTer22
NM_001370262.2:c.1594_1616del NP_001357191.2:p.Ala532HisfsTer22
NM_001370263.2:c.1594_1616del NP_001357192.2:p.Ala532HisfsTer22
NM_130799.3:c.1699_1721del NP_570711.2:p.Ala567HisfsTer22
NM_130800.3:c.1714_1736del NP_570712.2:p.Ala572HisfsTer22
NM_130801.3:c.1714_1736del NP_570713.2:p.Ala572HisfsTer22
NM_130802.3:c.1714_1736del NP_570714.2:p.Ala572HisfsTer22
NM_130803.3:c.1714_1736del NP_570715.2:p.Ala572HisfsTer22
NM_130804.3:c.1714_1736del NP_570716.2:p.Ala572HisfsTer22