Canonical Allele Identifier: CA1210236679

Gene: SOAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354438_179354440delinsCAT , CM000663.2:g.179354438_179354440delinsCAT	GRCh38
NC_000001.10:g.179323573_179323575delinsCAT , CM000663.1:g.179323573_179323575delinsCAT	GRCh37
NC_000001.9:g.177590196_177590198delinsCAT	NCBI36
NG_030638.1:g.65725_65727delinsCAT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*797_*799delinsCAT MANE Select	ENSP00000356591.3:n.*797_*799delinsCAT
ENST00000367619.7:c.*797_*799delinsCAT	ENSP00000356591.3:n.*797_*799delinsCAT
ENST00000539888.5:c.*797_*799delinsCAT	ENSP00000441356.1:n.*797_*799delinsCAT
ENST00000540564.5:c.*797_*799delinsCAT	ENSP00000445315.1:n.*797_*799delinsCAT
NM_001252511.1:c.*797_*799delinsCAT	NP_001239440.1:n.*797_*799delinsCAT
NM_001252512.1:c.*797_*799delinsCAT	NP_001239441.1:n.*797_*799delinsCAT
NM_003101.5:c.*797_*799delinsCAT	NP_003092.4:n.*797_*799delinsCAT
NR_045530.1:n.2600_2602delinsCAT
XM_011509911.1:c.*797_*799delinsCAT	XP_011508213.1:n.*797_*799delinsCAT
NM_003101.6:c.*797_*799delinsCAT MANE Select	NP_003092.4:n.*797_*799delinsCAT
NR_045530.2:n.2517_2519delinsCAT
NM_001252511.2:c.*797_*799delinsCAT	NP_001239440.1:n.*797_*799delinsCAT
NM_001252512.2:c.*797_*799delinsCAT	NP_001239441.1:n.*797_*799delinsCAT