Canonical Allele Identifier: CA2692653876

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674017-CACAGCCCCTCCCTGGGAAGCCCGAGGCCGGGCTCTTCCCCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674018_136674058del , CM000671.2:g.136674018_136674058del	GRCh38
NC_000009.11:g.139568470_139568510del , CM000671.1:g.139568470_139568510del	GRCh37
NC_000009.10:g.138688291_138688331del	NCBI36
NG_008090.1:g.18402_18442del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.662-131_662-91del MANE Select	ENSP00000360761.2:n.662-131_662-91del
ENST00000371694.7:c.566-131_566-91del	ENSP00000360759.3:n.566-131_566-91del
ENST00000371696.6:c.662-131_662-91del	ENSP00000360761.2:n.662-131_662-91del
ENST00000472820.1:n.590-131_590-91del
ENST00000538402.1:c.662-131_662-91del	ENSP00000438919.1:n.662-131_662-91del
NM_001012727.1:c.566-131_566-91del	NP_001012745.1:n.566-131_566-91del
NM_006412.3:c.662-131_662-91del	NP_006403.2:n.662-131_662-91del
NM_006412.4:c.662-131_662-91del MANE Select	NP_006403.2:n.662-131_662-91del
NM_001012727.2:c.566-131_566-91del	NP_001012745.1:n.566-131_566-91del