Canonical Allele Identifier: CA2692654297

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674851-GC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674853del , CM000671.2:g.136674853del	GRCh38
NC_000009.11:g.139569305del , CM000671.1:g.139569305del	GRCh37
NC_000009.10:g.138689126del	NCBI36
NG_008090.1:g.17608del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.589-45del MANE Select	ENSP00000360761.2:n.589-45del
ENST00000371694.7:c.493-45del	ENSP00000360759.3:n.493-45del
ENST00000371696.6:c.589-45del	ENSP00000360761.2:n.589-45del
ENST00000472820.1:n.517-45del
ENST00000538402.1:c.589-45del	ENSP00000438919.1:n.589-45del
NM_001012727.1:c.493-45del	NP_001012745.1:n.493-45del
NM_006412.3:c.589-45del	NP_006403.2:n.589-45del
NM_006412.4:c.589-45del MANE Select	NP_006403.2:n.589-45del
NM_001012727.2:c.493-45del	NP_001012745.1:n.493-45del