Canonical Allele Identifier: CA2692653939

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674071-CGTGGTGG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674074_136674080del , CM000671.2:g.136674074_136674080del	GRCh38
NC_000009.11:g.139568526_139568532del , CM000671.1:g.139568526_139568532del	GRCh37
NC_000009.10:g.138688347_138688353del	NCBI36
NG_008090.1:g.18382_18388del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.662-151_662-145del MANE Select	ENSP00000360761.2:n.662-151_662-145del
ENST00000371694.7:c.566-151_566-145del	ENSP00000360759.3:n.566-151_566-145del
ENST00000371696.6:c.662-151_662-145del	ENSP00000360761.2:n.662-151_662-145del
ENST00000472820.1:n.590-151_590-145del
ENST00000538402.1:c.662-151_662-145del	ENSP00000438919.1:n.662-151_662-145del
NM_001012727.1:c.566-151_566-145del	NP_001012745.1:n.566-151_566-145del
NM_006412.3:c.662-151_662-145del	NP_006403.2:n.662-151_662-145del
NM_006412.4:c.662-151_662-145del MANE Select	NP_006403.2:n.662-151_662-145del
NM_001012727.2:c.566-151_566-145del	NP_001012745.1:n.566-151_566-145del