Canonical Allele Identifier: CA2036816989

Gene: SOAT2

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
NM_003578.4:c.41A= MANE Select	NP_003569.1:p.Glu14=
ENST00000301466.8:c.41A= MANE Select	ENSP00000301466.3:p.Glu14=
NM_003578.3:c.41A=	NP_003569.1:p.Glu14=
ENST00000301466.7:c.41A=	ENSP00000301466.3:p.Glu14=
ENST00000542365.1:c.41A=	ENSP00000442234.1:p.Glu14=
ENST00000551896.5:c.41A=	ENSP00000450120.1:p.Glu14=
XM_011538849.1:c.41A=	XP_011537151.1:p.Glu14=
XM_011538850.1:c.41A=	XP_011537152.1:p.Glu14=
XM_011538851.1:c.41A=	XP_011537153.1:p.Glu14=
XR_944775.1:n.1014A=
XR_944777.1:n.1115A=
XR_944778.1:n.1019A=