Canonical Allele Identifier: CA381179139

Gene: MEN1

Linked Data

• ClinVar Variation Id: 1773237
• ClinVar RCV Id: RCV002396811
• MyVariant Identifiers: chr11:g.64572174G>C (hg19) ; chr11:g.64804702G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.64804702G>C , CM000673.2:g.64804702G>C	GRCh38
NC_000011.9:g.64572174G>C , CM000673.1:g.64572174G>C	GRCh37
NC_000011.8:g.64328750G>C	NCBI36
NG_008929.1:g.11593C>G , LRG_509:g.11593C>G
NG_033040.1:g.3540C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000377313.7:c.1480C>G	ENSP00000366530.1:p.Pro494Ala
ENST00000394374.8:c.*773C>G	ENSP00000377899.4:n.*773C>G
ENST00000394376.7:c.1456C>G	ENSP00000377901.3:p.Pro486Ala
ENST00000413626.2:c.1465C>G	ENSP00000411218.2:p.Pro489Ala
ENST00000424912.2:c.1465C>G	ENSP00000388016.2:p.Pro489Ala
ENST00000429702.6:c.1465C>G	ENSP00000402752.2:p.Pro489Ala
ENST00000672079.2:c.*561C>G	ENSP00000500905.2:n.*561C>G
ENST00000710881.1:c.1480C>G	ENSP00000518530.1:p.Pro494Ala
ENST00000394376.6:c.807C>G
ENST00000478548.3:n.1958C>G
ENST00000671939.2:n.1427C>G
ENST00000671965.2:n.1847C>G
ENST00000312049.11:c.1465C>G	ENSP00000308975.6:p.Pro489Ala
ENST00000315422.9:c.1465C>G	ENSP00000323747.4:p.Pro489Ala
ENST00000377313.6:c.1480C>G	ENSP00000366530.1:p.Pro494Ala
ENST00000440873.6:c.1465C>G	ENSP00000413944.2:p.Pro489Ala
ENST00000450708.7:c.1465C>G MANE Select	ENSP00000394933.3:p.Pro489Ala
ENST00000478548.2:n.1966C>G
ENST00000671939.1:n.1742C>G
ENST00000672304.1:c.1591C>G	ENSP00000500585.1:p.Pro531Ala
ENST00000312049.10:c.1465C>G	ENSP00000308975.6:p.Pro489Ala
ENST00000315422.8:c.1465C>G	ENSP00000323747.4:p.Pro489Ala
ENST00000337652.5:c.1480C>G	ENSP00000337088.1:p.Pro494Ala
ENST00000377313.5:c.1480C>G	ENSP00000366530.1:p.Pro494Ala
ENST00000377316.6:c.1300C>G	ENSP00000366533.1:p.Pro434Ala
ENST00000377321.5:c.1360C>G	ENSP00000366538.1:p.Pro454Ala
ENST00000377326.7:c.1465C>G	ENSP00000366543.3:p.Pro489Ala
ENST00000394374.6:c.1480C>G	ENSP00000377899.2:p.Pro494Ala
ENST00000394376.5:c.1480C>G	ENSP00000377901.1:p.Pro494Ala
ENST00000478548.1:n.1014C>G
NM_000244.3:c.1480C>G , LRG_509t1:c.1480C>G	NP_000235.2:p.Pro494Ala
NM_130799.2:c.1465C>G , LRG_509t2:c.1465C>G	NP_570711.1:p.Pro489Ala
NM_130800.2:c.1480C>G	NP_570712.1:p.Pro494Ala
NM_130801.2:c.1480C>G	NP_570713.1:p.Pro494Ala
NM_130802.2:c.1480C>G	NP_570714.1:p.Pro494Ala
NM_130803.2:c.1480C>G	NP_570715.1:p.Pro494Ala
NM_130804.2:c.1480C>G	NP_570716.1:p.Pro494Ala
XM_005274001.3:c.1465C>G	XP_005274058.1:p.Pro489Ala
XM_011545040.1:c.1591C>G	XP_011543342.1:p.Pro531Ala
XM_011545041.1:c.1591C>G	XP_011543343.1:p.Pro531Ala
XM_011545042.1:c.1591C>G	XP_011543344.1:p.Pro531Ala
XM_005274001.4:c.1465C>G	XP_005274058.1:p.Pro489Ala
XM_011545041.2:c.1591C>G	XP_011543343.1:p.Pro531Ala
XM_011545042.3:c.1591C>G	XP_011543344.1:p.Pro531Ala
XM_017017765.1:c.1606C>G	XP_016873254.1:p.Pro536Ala
XM_017017766.1:c.1606C>G	XP_016873255.1:p.Pro536Ala
XM_017017767.2:c.1606C>G	XP_016873256.1:p.Pro536Ala
XM_017017768.1:c.1606C>G	XP_016873257.1:p.Pro536Ala
XM_017017769.1:c.1465C>G	XP_016873258.1:p.Pro489Ala
XM_017017770.2:c.1465C>G	XP_016873259.1:p.Pro489Ala
NM_001370251.1:c.1591C>G	NP_001357180.1:p.Pro531Ala
NM_001370259.2:c.1465C>G MANE Select	NP_001357188.2:p.Pro489Ala
NM_001370260.1:c.1465C>G	NP_001357189.1:p.Pro489Ala
NM_001370261.1:c.1465C>G	NP_001357190.1:p.Pro489Ala
NM_001370262.1:c.1360C>G	NP_001357191.1:p.Pro454Ala
NM_001370263.1:c.1360C>G	NP_001357192.1:p.Pro454Ala
NM_000244.4:c.1480C>G	NP_000235.3:p.Pro494Ala
NM_001370251.2:c.1591C>G	NP_001357180.2:p.Pro531Ala
NM_001370260.2:c.1465C>G	NP_001357189.2:p.Pro489Ala
NM_001370261.2:c.1465C>G	NP_001357190.2:p.Pro489Ala
NM_001370262.2:c.1360C>G	NP_001357191.2:p.Pro454Ala
NM_001370263.2:c.1360C>G	NP_001357192.2:p.Pro454Ala
NM_130799.3:c.1465C>G	NP_570711.2:p.Pro489Ala
NM_130800.3:c.1480C>G	NP_570712.2:p.Pro494Ala
NM_130801.3:c.1480C>G	NP_570713.2:p.Pro494Ala
NM_130802.3:c.1480C>G	NP_570714.2:p.Pro494Ala
NM_130803.3:c.1480C>G	NP_570715.2:p.Pro494Ala
NM_130804.3:c.1480C>G	NP_570716.2:p.Pro494Ala