Canonical Allele Identifier: CA1210236639

Gene: SOAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354325T= , CM000663.2:g.179354325T=	GRCh38
NC_000001.10:g.179323460T= , CM000663.1:g.179323460T=	GRCh37
NC_000001.9:g.177590083T=	NCBI36
NG_030638.1:g.65612T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*684T= MANE Select	ENSP00000356591.3:n.*684T=
ENST00000367619.7:c.*684T=	ENSP00000356591.3:n.*684T=
ENST00000539888.5:c.*684T=	ENSP00000441356.1:n.*684T=
ENST00000540564.5:c.*684T=	ENSP00000445315.1:n.*684T=
NM_001252511.1:c.*684T=	NP_001239440.1:n.*684T=
NM_001252512.1:c.*684T=	NP_001239441.1:n.*684T=
NM_003101.5:c.*684T=	NP_003092.4:n.*684T=
NR_045530.1:n.2487T=
XM_011509911.1:c.*684T=	XP_011508213.1:n.*684T=
NM_003101.6:c.*684T= MANE Select	NP_003092.4:n.*684T=
NR_045530.2:n.2404T=
NM_001252511.2:c.*684T=	NP_001239440.1:n.*684T=
NM_001252512.2:c.*684T=	NP_001239441.1:n.*684T=