Canonical Allele Identifier: CA1210236699

Gene: SOAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354492C= , CM000663.2:g.179354492C=	GRCh38
NC_000001.10:g.179323627C= , CM000663.1:g.179323627C=	GRCh37
NC_000001.9:g.177590250C=	NCBI36
NG_030638.1:g.65779C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*851C= MANE Select	ENSP00000356591.3:n.*851C=
ENST00000367619.7:c.*851C=	ENSP00000356591.3:n.*851C=
ENST00000539888.5:c.*851C=	ENSP00000441356.1:n.*851C=
ENST00000540564.5:c.*851C=	ENSP00000445315.1:n.*851C=
NM_001252511.1:c.*851C=	NP_001239440.1:n.*851C=
NM_001252512.1:c.*851C=	NP_001239441.1:n.*851C=
NM_003101.5:c.*851C=	NP_003092.4:n.*851C=
NR_045530.1:n.2654C=
XM_011509911.1:c.*851C=	XP_011508213.1:n.*851C=
NM_003101.6:c.*851C= MANE Select	NP_003092.4:n.*851C=
NR_045530.2:n.2571C=
NM_001252511.2:c.*851C=	NP_001239440.1:n.*851C=
NM_001252512.2:c.*851C=	NP_001239441.1:n.*851C=