Canonical Allele Identifier: CA1210236693
Gene: SOAT1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000001.11:g.179354469A= , CM000663.2:g.179354469A= GRCh38
NC_000001.10:g.179323604A= , CM000663.1:g.179323604A= GRCh37
NC_000001.9:g.177590227A= NCBI36
NG_030638.1:g.65756A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000367619.8:c.*828A= MANE Select ENSP00000356591.3:n.*828A=
ENST00000367619.7:c.*828A= ENSP00000356591.3:n.*828A=
ENST00000539888.5:c.*828A= ENSP00000441356.1:n.*828A=
ENST00000540564.5:c.*828A= ENSP00000445315.1:n.*828A=
NM_001252511.1:c.*828A= NP_001239440.1:n.*828A=
NM_001252512.1:c.*828A= NP_001239441.1:n.*828A=
NM_003101.5:c.*828A= NP_003092.4:n.*828A=
NR_045530.1:n.2631A=
XM_011509911.1:c.*828A= XP_011508213.1:n.*828A=
NM_003101.6:c.*828A= MANE Select NP_003092.4:n.*828A=
NR_045530.2:n.2548A=
NM_001252511.2:c.*828A= NP_001239440.1:n.*828A=
NM_001252512.2:c.*828A= NP_001239441.1:n.*828A=