Canonical Allele Identifier: CA891805039

Gene: SOAT1

Linked Data

• dbSNP Id: rs1234552530
• MyVariant Identifiers: chr1:g.179323470_179323471insAGTAGGAAGTAGGAAG (hg19) ; chr1:g.179354335_179354336insAGTAGGAAGTAGGAAG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354335_179354336insAGTAGGAAGTAGGAAG , CM000663.2:g.179354335_179354336insAGTAGGAAGTAGGAAG	GRCh38
NC_000001.10:g.179323470_179323471insAGTAGGAAGTAGGAAG , CM000663.1:g.179323470_179323471insAGTAGGAAGTAGGAAG	GRCh37
NC_000001.9:g.177590093_177590094insAGTAGGAAGTAGGAAG	NCBI36
NG_030638.1:g.65622_65623insAGTAGGAAGTAGGAAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*694_*695insAGTAGGAAGTAGGAAG MANE Select	ENSP00000356591.3:n.*694_*695insAGTAGGAAGTAGGAAG
ENST00000367619.7:c.*694_*695insAGTAGGAAGTAGGAAG	ENSP00000356591.3:n.*694_*695insAGTAGGAAGTAGGAAG
ENST00000539888.5:c.*694_*695insAGTAGGAAGTAGGAAG	ENSP00000441356.1:n.*694_*695insAGTAGGAAGTAGGAAG
ENST00000540564.5:c.*694_*695insAGTAGGAAGTAGGAAG	ENSP00000445315.1:n.*694_*695insAGTAGGAAGTAGGAAG
NM_001252511.1:c.*694_*695insAGTAGGAAGTAGGAAG	NP_001239440.1:n.*694_*695insAGTAGGAAGTAGGAAG
NM_001252512.1:c.*694_*695insAGTAGGAAGTAGGAAG	NP_001239441.1:n.*694_*695insAGTAGGAAGTAGGAAG
NM_003101.5:c.*694_*695insAGTAGGAAGTAGGAAG	NP_003092.4:n.*694_*695insAGTAGGAAGTAGGAAG
NR_045530.1:n.2497_2498insAGTAGGAAGTAGGAAG
XM_011509911.1:c.*694_*695insAGTAGGAAGTAGGAAG	XP_011508213.1:n.*694_*695insAGTAGGAAGTAGGAAG
NM_003101.6:c.*694_*695insAGTAGGAAGTAGGAAG MANE Select	NP_003092.4:n.*694_*695insAGTAGGAAGTAGGAAG
NR_045530.2:n.2414_2415insAGTAGGAAGTAGGAAG
NM_001252511.2:c.*694_*695insAGTAGGAAGTAGGAAG	NP_001239440.1:n.*694_*695insAGTAGGAAGTAGGAAG
NM_001252512.2:c.*694_*695insAGTAGGAAGTAGGAAG	NP_001239441.1:n.*694_*695insAGTAGGAAGTAGGAAG