Canonical Allele Identifier: CA2720874523

Gene: AGPAT2

Linked Data

• dbSNP Id: rs2119178208

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674077_136674080del , CM000671.2:g.136674077_136674080del	GRCh38
NC_000009.11:g.139568529_139568532del , CM000671.1:g.139568529_139568532del	GRCh37
NC_000009.10:g.138688350_138688353del	NCBI36
NG_008090.1:g.18383_18386del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.662-150_662-147del MANE Select	ENSP00000360761.2:n.662-150_662-147del
ENST00000371694.7:c.566-150_566-147del	ENSP00000360759.3:n.566-150_566-147del
ENST00000371696.6:c.662-150_662-147del	ENSP00000360761.2:n.662-150_662-147del
ENST00000472820.1:n.590-150_590-147del
ENST00000538402.1:c.662-150_662-147del	ENSP00000438919.1:n.662-150_662-147del
NM_001012727.1:c.566-150_566-147del	NP_001012745.1:n.566-150_566-147del
NM_006412.3:c.662-150_662-147del	NP_006403.2:n.662-150_662-147del
NM_006412.4:c.662-150_662-147del MANE Select	NP_006403.2:n.662-150_662-147del
NM_001012727.2:c.566-150_566-147del	NP_001012745.1:n.566-150_566-147del