Canonical Allele Identifier: CA1210236589

Gene: SOAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354194_179354195delinsAT , CM000663.2:g.179354194_179354195delinsAT	GRCh38
NC_000001.10:g.179323329_179323330delinsAT , CM000663.1:g.179323329_179323330delinsAT	GRCh37
NC_000001.9:g.177589952_177589953delinsAT	NCBI36
NG_030638.1:g.65481_65482delinsAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*553_*554delinsAT MANE Select	ENSP00000356591.3:n.*553_*554delinsAT
ENST00000367619.7:c.*553_*554delinsAT	ENSP00000356591.3:n.*553_*554delinsAT
ENST00000539888.5:c.*553_*554delinsAT	ENSP00000441356.1:n.*553_*554delinsAT
ENST00000540564.5:c.*553_*554delinsAT	ENSP00000445315.1:n.*553_*554delinsAT
NM_001252511.1:c.*553_*554delinsAT	NP_001239440.1:n.*553_*554delinsAT
NM_001252512.1:c.*553_*554delinsAT	NP_001239441.1:n.*553_*554delinsAT
NM_003101.5:c.*553_*554delinsAT	NP_003092.4:n.*553_*554delinsAT
NR_045530.1:n.2356_2357delinsAT
XM_011509911.1:c.*553_*554delinsAT	XP_011508213.1:n.*553_*554delinsAT
NM_003101.6:c.*553_*554delinsAT MANE Select	NP_003092.4:n.*553_*554delinsAT
NR_045530.2:n.2273_2274delinsAT
NM_001252511.2:c.*553_*554delinsAT	NP_001239440.1:n.*553_*554delinsAT
NM_001252512.2:c.*553_*554delinsAT	NP_001239441.1:n.*553_*554delinsAT