Canonical Allele Identifier: CA1009659537

Gene: SOAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354208_179354209insAAAAAAAA , CM000663.2:g.179354208_179354209insAAAAAAAA	GRCh38
NC_000001.10:g.179323343_179323344insAAAAAAAA , CM000663.1:g.179323343_179323344insAAAAAAAA	GRCh37
NC_000001.9:g.177589966_177589967insAAAAAAAA	NCBI36
NG_030638.1:g.65495_65496insAAAAAAAA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*567_*568insAAAAAAAA MANE Select	ENSP00000356591.3:n.*567_*568insAAAAAAAA
ENST00000367619.7:c.*567_*568insAAAAAAAA	ENSP00000356591.3:n.*567_*568insAAAAAAAA
ENST00000539888.5:c.*567_*568insAAAAAAAA	ENSP00000441356.1:n.*567_*568insAAAAAAAA
ENST00000540564.5:c.*567_*568insAAAAAAAA	ENSP00000445315.1:n.*567_*568insAAAAAAAA
NM_001252511.1:c.*567_*568insAAAAAAAA	NP_001239440.1:n.*567_*568insAAAAAAAA
NM_001252512.1:c.*567_*568insAAAAAAAA	NP_001239441.1:n.*567_*568insAAAAAAAA
NM_003101.5:c.*567_*568insAAAAAAAA	NP_003092.4:n.*567_*568insAAAAAAAA
NR_045530.1:n.2370_2371insAAAAAAAA
XM_011509911.1:c.*567_*568insAAAAAAAA	XP_011508213.1:n.*567_*568insAAAAAAAA
NM_003101.6:c.*567_*568insAAAAAAAA MANE Select	NP_003092.4:n.*567_*568insAAAAAAAA
NR_045530.2:n.2287_2288insAAAAAAAA
NM_001252511.2:c.*567_*568insAAAAAAAA	NP_001239440.1:n.*567_*568insAAAAAAAA
NM_001252512.2:c.*567_*568insAAAAAAAA	NP_001239441.1:n.*567_*568insAAAAAAAA