Canonical Allele Identifier: CA1140439200

Gene: SOAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179351443A= , CM000663.2:g.179351443A=	GRCh38
NC_000001.10:g.179320578A= , CM000663.1:g.179320578A=	GRCh37
NC_000001.9:g.177587201A=	NCBI36
NG_030638.1:g.62730A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.1577A= MANE Select	ENSP00000356591.3:p.Gln526=
ENST00000367619.7:c.1577A=	ENSP00000356591.3:p.Gln526=
ENST00000539888.5:c.1382A=	ENSP00000441356.1:p.Gln461=
ENST00000540564.5:c.1403A=	ENSP00000445315.1:p.Gln468=
NM_001252511.1:c.1403A=	NP_001239440.1:p.Gln468=
NM_001252512.1:c.1382A=	NP_001239441.1:p.Gln461=
NM_003101.5:c.1577A=	NP_003092.4:p.Gln526=
NR_045530.1:n.1727A=
XM_011509911.1:c.1577A=	XP_011508213.1:p.Gln526=
NM_003101.6:c.1577A= MANE Select	NP_003092.4:p.Gln526=
NR_045530.2:n.1644A=
NM_001252511.2:c.1403A=	NP_001239440.1:p.Gln468=
NM_001252512.2:c.1382A=	NP_001239441.1:p.Gln461=