Canonical Allele Identifier: CA6593762

Gene: SOAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.53103618A>G , CM000674.2:g.53103618A>G	GRCh38
NC_000012.11:g.53497402A>G , CM000674.1:g.53497402A>G	GRCh37
NC_000012.10:g.51783669A>G	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_003578.4:c.41A>G MANE Select	NP_003569.1:p.Glu14Gly
ENST00000301466.8:c.41A>G MANE Select	ENSP00000301466.3:p.Glu14Gly
NM_003578.3:c.41A>G	NP_003569.1:p.Glu14Gly
ENST00000301466.7:c.41A>G	ENSP00000301466.3:p.Glu14Gly
ENST00000542365.1:c.41A>G	ENSP00000442234.1:p.Glu14Gly
ENST00000551896.5:c.41A>G	ENSP00000450120.1:p.Glu14Gly
XM_011538849.1:c.41A>G	XP_011537151.1:p.Glu14Gly
XM_011538850.1:c.41A>G	XP_011537152.1:p.Glu14Gly
XM_011538851.1:c.41A>G	XP_011537153.1:p.Glu14Gly
XR_944775.1:n.1014A>G
XR_944777.1:n.1115A>G
XR_944778.1:n.1019A>G