Canonical Allele Identifier: CA1210236719

Gene: SOAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354552C= , CM000663.2:g.179354552C=	GRCh38
NC_000001.10:g.179323687C= , CM000663.1:g.179323687C=	GRCh37
NC_000001.9:g.177590310C=	NCBI36
NG_030638.1:g.65839C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*911C= MANE Select	ENSP00000356591.3:n.*911C=
ENST00000367619.7:c.*911C=	ENSP00000356591.3:n.*911C=
ENST00000539888.5:c.*911C=	ENSP00000441356.1:n.*911C=
ENST00000540564.5:c.*911C=	ENSP00000445315.1:n.*911C=
NM_001252511.1:c.*911C=	NP_001239440.1:n.*911C=
NM_001252512.1:c.*911C=	NP_001239441.1:n.*911C=
NM_003101.5:c.*911C=	NP_003092.4:n.*911C=
NR_045530.1:n.2714C=
XM_011509911.1:c.*911C=	XP_011508213.1:n.*911C=
NM_003101.6:c.*911C= MANE Select	NP_003092.4:n.*911C=
NR_045530.2:n.2631C=
NM_001252511.2:c.*911C=	NP_001239440.1:n.*911C=
NM_001252512.2:c.*911C=	NP_001239441.1:n.*911C=