Canonical Allele Identifier: CA2566278934

Gene: SOAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354218_179354219insTTT , CM000663.2:g.179354218_179354219insTTT	GRCh38
NC_000001.10:g.179323353_179323354insTTT , CM000663.1:g.179323353_179323354insTTT	GRCh37
NC_000001.9:g.177589976_177589977insTTT	NCBI36
NG_030638.1:g.65505_65506insTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*577_*578insTTT MANE Select	ENSP00000356591.3:n.*577_*578insTTT
ENST00000367619.7:c.*577_*578insTTT	ENSP00000356591.3:n.*577_*578insTTT
ENST00000539888.5:c.*577_*578insTTT	ENSP00000441356.1:n.*577_*578insTTT
ENST00000540564.5:c.*577_*578insTTT	ENSP00000445315.1:n.*577_*578insTTT
NM_001252511.1:c.*577_*578insTTT	NP_001239440.1:n.*577_*578insTTT
NM_001252512.1:c.*577_*578insTTT	NP_001239441.1:n.*577_*578insTTT
NM_003101.5:c.*577_*578insTTT	NP_003092.4:n.*577_*578insTTT
NR_045530.1:n.2380_2381insTTT
XM_011509911.1:c.*577_*578insTTT	XP_011508213.1:n.*577_*578insTTT
NM_003101.6:c.*577_*578insTTT MANE Select	NP_003092.4:n.*577_*578insTTT
NR_045530.2:n.2297_2298insTTT
NM_001252511.2:c.*577_*578insTTT	NP_001239440.1:n.*577_*578insTTT
NM_001252512.2:c.*577_*578insTTT	NP_001239441.1:n.*577_*578insTTT