Canonical Allele Identifier: CA502427

Gene: SAMD11

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.930201C>T , CM000663.2:g.930201C>T	GRCh38
NC_000001.10:g.865581C>T , CM000663.1:g.865581C>T	GRCh37
NC_000001.9:g.855444C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000342066.8:c.119C>T	ENSP00000342313.3:p.Ala40Val
ENST00000616016.5:c.656C>T MANE Select	ENSP00000478421.2:p.Ala219Val
ENST00000616125.5:c.119C>T	ENSP00000484643.1:p.Ala40Val
ENST00000617307.5:c.119C>T	ENSP00000482090.2:p.Ala40Val
ENST00000618181.5:c.119C>T	ENSP00000480870.1:p.Ala40Val
ENST00000618323.5:c.656C>T	ENSP00000480678.2:p.Ala219Val
ENST00000618779.5:c.119C>T	ENSP00000484256.1:p.Ala40Val
ENST00000622503.5:c.119C>T	ENSP00000482138.1:p.Ala40Val
ENST00000342066.7:c.119C>T	ENSP00000342313.3:p.Ala40Val
ENST00000420190.5:c.119C>T	ENSP00000411579.1:p.Ala40Val
ENST00000437963.5:c.119C>T	ENSP00000393181.1:p.Ala40Val
ENST00000616016.4:c.119C>T	ENSP00000478421.1:p.Ala40Val
ENST00000616125.4:c.119C>T	ENSP00000484643.1:p.Ala40Val
ENST00000617307.4:c.119C>T	ENSP00000482090.1:p.Ala40Val
ENST00000618181.4:c.119C>T	ENSP00000480870.1:p.Ala40Val
ENST00000618323.4:c.119C>T	ENSP00000480678.1:p.Ala40Val
ENST00000618779.4:c.119C>T	ENSP00000484256.1:p.Ala40Val
ENST00000620200.4:c.119C>T	ENSP00000484820.1:p.Ala40Val
ENST00000622503.4:c.119C>T	ENSP00000482138.1:p.Ala40Val
NM_152486.2:c.119C>T	NP_689699.2:p.Ala40Val
NM_152486.3:c.119C>T	NP_689699.2:p.Ala40Val
NM_001385640.1:c.656C>T	NP_001372569.1:p.Ala219Val
NM_001385641.1:c.656C>T MANE Select	NP_001372570.1:p.Ala219Val
NM_152486.4:c.119C>T	NP_689699.3:p.Ala40Val