Canonical Allele Identifier: CA1210236739

Gene: SOAT1

Linked Data

• dbSNP Id: rs1571464996

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354580T>C , CM000663.2:g.179354580T>C	GRCh38
NC_000001.10:g.179323715T>C , CM000663.1:g.179323715T>C	GRCh37
NC_000001.9:g.177590338T>C	NCBI36
NG_030638.1:g.65867T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*939T>C MANE Select	ENSP00000356591.3:n.*939T>C
ENST00000367619.7:c.*939T>C	ENSP00000356591.3:n.*939T>C
ENST00000539888.5:c.*939T>C	ENSP00000441356.1:n.*939T>C
ENST00000540564.5:c.*939T>C	ENSP00000445315.1:n.*939T>C
NM_001252511.1:c.*939T>C	NP_001239440.1:n.*939T>C
NM_001252512.1:c.*939T>C	NP_001239441.1:n.*939T>C
NM_003101.5:c.*939T>C	NP_003092.4:n.*939T>C
NR_045530.1:n.2742T>C
XM_011509911.1:c.*939T>C	XP_011508213.1:n.*939T>C
NM_003101.6:c.*939T>C MANE Select	NP_003092.4:n.*939T>C
NR_045530.2:n.2659T>C
NM_001252511.2:c.*939T>C	NP_001239440.1:n.*939T>C
NM_001252512.2:c.*939T>C	NP_001239441.1:n.*939T>C