Canonical Allele Identifier: CA1210236711

Gene: SOAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354538_179354541delinsAATT , CM000663.2:g.179354538_179354541delinsAATT	GRCh38
NC_000001.10:g.179323673_179323676delinsAATT , CM000663.1:g.179323673_179323676delinsAATT	GRCh37
NC_000001.9:g.177590296_177590299delinsAATT	NCBI36
NG_030638.1:g.65825_65828delinsAATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*897_*900delinsAATT MANE Select	ENSP00000356591.3:n.*897_*900delinsAATT
ENST00000367619.7:c.*897_*900delinsAATT	ENSP00000356591.3:n.*897_*900delinsAATT
ENST00000539888.5:c.*897_*900delinsAATT	ENSP00000441356.1:n.*897_*900delinsAATT
ENST00000540564.5:c.*897_*900delinsAATT	ENSP00000445315.1:n.*897_*900delinsAATT
NM_001252511.1:c.*897_*900delinsAATT	NP_001239440.1:n.*897_*900delinsAATT
NM_001252512.1:c.*897_*900delinsAATT	NP_001239441.1:n.*897_*900delinsAATT
NM_003101.5:c.*897_*900delinsAATT	NP_003092.4:n.*897_*900delinsAATT
NR_045530.1:n.2700_2703delinsAATT
XM_011509911.1:c.*897_*900delinsAATT	XP_011508213.1:n.*897_*900delinsAATT
NM_003101.6:c.*897_*900delinsAATT MANE Select	NP_003092.4:n.*897_*900delinsAATT
NR_045530.2:n.2617_2620delinsAATT
NM_001252511.2:c.*897_*900delinsAATT	NP_001239440.1:n.*897_*900delinsAATT
NM_001252512.2:c.*897_*900delinsAATT	NP_001239441.1:n.*897_*900delinsAATT