Canonical Allele Identifier: CA1210236590

Gene: SOAT1

Linked Data

• dbSNP Id: rs1666838037
• gnomAD v4: 1-179354194-A-T

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354194A>T , CM000663.2:g.179354194A>T	GRCh38
NC_000001.10:g.179323329A>T , CM000663.1:g.179323329A>T	GRCh37
NC_000001.9:g.177589952A>T	NCBI36
NG_030638.1:g.65481A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*553A>T MANE Select	ENSP00000356591.3:n.*553A>T
ENST00000367619.7:c.*553A>T	ENSP00000356591.3:n.*553A>T
ENST00000539888.5:c.*553A>T	ENSP00000441356.1:n.*553A>T
ENST00000540564.5:c.*553A>T	ENSP00000445315.1:n.*553A>T
NM_001252511.1:c.*553A>T	NP_001239440.1:n.*553A>T
NM_001252512.1:c.*553A>T	NP_001239441.1:n.*553A>T
NM_003101.5:c.*553A>T	NP_003092.4:n.*553A>T
NR_045530.1:n.2356A>T
XM_011509911.1:c.*553A>T	XP_011508213.1:n.*553A>T
NM_003101.6:c.*553A>T MANE Select	NP_003092.4:n.*553A>T
NR_045530.2:n.2273A>T
NM_001252511.2:c.*553A>T	NP_001239440.1:n.*553A>T
NM_001252512.2:c.*553A>T	NP_001239441.1:n.*553A>T