Canonical Allele Identifier: CA2649304906

Gene: SOAT1

Linked Data

• gnomAD v4: 1-179354269-G-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354269G>T , CM000663.2:g.179354269G>T	GRCh38
NC_000001.10:g.179323404G>T , CM000663.1:g.179323404G>T	GRCh37
NC_000001.9:g.177590027G>T	NCBI36
NG_030638.1:g.65556G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*628G>T MANE Select	ENSP00000356591.3:n.*628G>T
ENST00000367619.7:c.*628G>T	ENSP00000356591.3:n.*628G>T
ENST00000539888.5:c.*628G>T	ENSP00000441356.1:n.*628G>T
ENST00000540564.5:c.*628G>T	ENSP00000445315.1:n.*628G>T
NM_001252511.1:c.*628G>T	NP_001239440.1:n.*628G>T
NM_001252512.1:c.*628G>T	NP_001239441.1:n.*628G>T
NM_003101.5:c.*628G>T	NP_003092.4:n.*628G>T
NR_045530.1:n.2431G>T
XM_011509911.1:c.*628G>T	XP_011508213.1:n.*628G>T
NM_003101.6:c.*628G>T MANE Select	NP_003092.4:n.*628G>T
NR_045530.2:n.2348G>T
NM_001252511.2:c.*628G>T	NP_001239440.1:n.*628G>T
NM_001252512.2:c.*628G>T	NP_001239441.1:n.*628G>T