Canonical Allele Identifier: CA2746816767

Gene: SOAT1

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.179354297_179354298del , CM000663.2:g.179354297_179354298del	GRCh38
NC_000001.10:g.179323432_179323433del , CM000663.1:g.179323432_179323433del	GRCh37
NC_000001.9:g.177590055_177590056del	NCBI36
NG_030638.1:g.65584_65585del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000367619.8:c.*656_*657del MANE Select	ENSP00000356591.3:n.*656_*657del
ENST00000367619.7:c.*656_*657del	ENSP00000356591.3:n.*656_*657del
ENST00000539888.5:c.*656_*657del	ENSP00000441356.1:n.*656_*657del
ENST00000540564.5:c.*656_*657del	ENSP00000445315.1:n.*656_*657del
NM_001252511.1:c.*656_*657del	NP_001239440.1:n.*656_*657del
NM_001252512.1:c.*656_*657del	NP_001239441.1:n.*656_*657del
NM_003101.5:c.*656_*657del	NP_003092.4:n.*656_*657del
NR_045530.1:n.2459_2460del
XM_011509911.1:c.*656_*657del	XP_011508213.1:n.*656_*657del
NM_003101.6:c.*656_*657del MANE Select	NP_003092.4:n.*656_*657del
NR_045530.2:n.2376_2377del
NM_001252511.2:c.*656_*657del	NP_001239440.1:n.*656_*657del
NM_001252512.2:c.*656_*657del	NP_001239441.1:n.*656_*657del