Canonical Allele Identifier: CA1210236692

Gene: SOAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354465_179354467delinsCTT , CM000663.2:g.179354465_179354467delinsCTT	GRCh38
NC_000001.10:g.179323600_179323602delinsCTT , CM000663.1:g.179323600_179323602delinsCTT	GRCh37
NC_000001.9:g.177590223_177590225delinsCTT	NCBI36
NG_030638.1:g.65752_65754delinsCTT

Transcript Alleles

HGVS	Amino-acid change
ENST00000367619.8:c.*824_*826delinsCTT MANE Select	ENSP00000356591.3:n.*824_*826delinsCTT
ENST00000367619.7:c.*824_*826delinsCTT	ENSP00000356591.3:n.*824_*826delinsCTT
ENST00000539888.5:c.*824_*826delinsCTT	ENSP00000441356.1:n.*824_*826delinsCTT
ENST00000540564.5:c.*824_*826delinsCTT	ENSP00000445315.1:n.*824_*826delinsCTT
NM_001252511.1:c.*824_*826delinsCTT	NP_001239440.1:n.*824_*826delinsCTT
NM_001252512.1:c.*824_*826delinsCTT	NP_001239441.1:n.*824_*826delinsCTT
NM_003101.5:c.*824_*826delinsCTT	NP_003092.4:n.*824_*826delinsCTT
NR_045530.1:n.2627_2629delinsCTT
XM_011509911.1:c.*824_*826delinsCTT	XP_011508213.1:n.*824_*826delinsCTT
NM_003101.6:c.*824_*826delinsCTT MANE Select	NP_003092.4:n.*824_*826delinsCTT
NR_045530.2:n.2544_2546delinsCTT
NM_001252511.2:c.*824_*826delinsCTT	NP_001239440.1:n.*824_*826delinsCTT
NM_001252512.2:c.*824_*826delinsCTT	NP_001239441.1:n.*824_*826delinsCTT