Canonical Allele Identifier: CA2527582529

Gene: SOAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354269_179354270insGCC , CM000663.2:g.179354269_179354270insGCC	GRCh38
NC_000001.10:g.179323404_179323405insGCC , CM000663.1:g.179323404_179323405insGCC	GRCh37
NC_000001.9:g.177590027_177590028insGCC	NCBI36
NG_030638.1:g.65556_65557insGCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*628_*629insGCC MANE Select	ENSP00000356591.3:n.*628_*629insGCC
ENST00000367619.7:c.*628_*629insGCC	ENSP00000356591.3:n.*628_*629insGCC
ENST00000539888.5:c.*628_*629insGCC	ENSP00000441356.1:n.*628_*629insGCC
ENST00000540564.5:c.*628_*629insGCC	ENSP00000445315.1:n.*628_*629insGCC
NM_001252511.1:c.*628_*629insGCC	NP_001239440.1:n.*628_*629insGCC
NM_001252512.1:c.*628_*629insGCC	NP_001239441.1:n.*628_*629insGCC
NM_003101.5:c.*628_*629insGCC	NP_003092.4:n.*628_*629insGCC
NR_045530.1:n.2431_2432insGCC
XM_011509911.1:c.*628_*629insGCC	XP_011508213.1:n.*628_*629insGCC
NM_003101.6:c.*628_*629insGCC MANE Select	NP_003092.4:n.*628_*629insGCC
NR_045530.2:n.2348_2349insGCC
NM_001252511.2:c.*628_*629insGCC	NP_001239440.1:n.*628_*629insGCC
NM_001252512.2:c.*628_*629insGCC	NP_001239441.1:n.*628_*629insGCC