Canonical Allele Identifier: CA1210236707
Gene: SOAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179354513G= , CM000663.2:g.179354513G= GRCh38
NC_000001.10:g.179323648G= , CM000663.1:g.179323648G= GRCh37
NC_000001.9:g.177590271G= NCBI36
NG_030638.1:g.65800G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367619.8:c.*872G= MANE Select ENSP00000356591.3:n.*872G=
ENST00000367619.7:c.*872G= ENSP00000356591.3:n.*872G=
ENST00000539888.5:c.*872G= ENSP00000441356.1:n.*872G=
ENST00000540564.5:c.*872G= ENSP00000445315.1:n.*872G=
NM_001252511.1:c.*872G= NP_001239440.1:n.*872G=
NM_001252512.1:c.*872G= NP_001239441.1:n.*872G=
NM_003101.5:c.*872G= NP_003092.4:n.*872G=
NR_045530.1:n.2675G=
XM_011509911.1:c.*872G= XP_011508213.1:n.*872G=
NM_003101.6:c.*872G= MANE Select NP_003092.4:n.*872G=
NR_045530.2:n.2592G=
NM_001252511.2:c.*872G= NP_001239440.1:n.*872G=
NM_001252512.2:c.*872G= NP_001239441.1:n.*872G=