Canonical Allele Identifier: CA2692654363

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674896-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674898dup , CM000671.2:g.136674898dup	GRCh38
NC_000009.11:g.139569350dup , CM000671.1:g.139569350dup	GRCh37
NC_000009.10:g.138689171dup	NCBI36
NG_008090.1:g.17563dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.589-90dup MANE Select	ENSP00000360761.2:n.589-90dup
ENST00000371694.7:c.493-90dup	ENSP00000360759.3:n.493-90dup
ENST00000371696.6:c.589-90dup	ENSP00000360761.2:n.589-90dup
ENST00000472820.1:n.517-90dup
ENST00000538402.1:c.589-90dup	ENSP00000438919.1:n.589-90dup
NM_001012727.1:c.493-90dup	NP_001012745.1:n.493-90dup
NM_006412.3:c.589-90dup	NP_006403.2:n.589-90dup
NM_006412.4:c.589-90dup MANE Select	NP_006403.2:n.589-90dup
NM_001012727.2:c.493-90dup	NP_001012745.1:n.493-90dup