Canonical Allele Identifier: CA2579519925

Gene: AGPAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674845_136674846del , CM000671.2:g.136674845_136674846del	GRCh38
NC_000009.11:g.139569297_139569298del , CM000671.1:g.139569297_139569298del	GRCh37
NC_000009.10:g.138689118_138689119del	NCBI36
NG_008090.1:g.17616_17617del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.589-37_589-36del MANE Select	ENSP00000360761.2:n.589-37_589-36del
ENST00000371694.7:c.493-37_493-36del	ENSP00000360759.3:n.493-37_493-36del
ENST00000371696.6:c.589-37_589-36del	ENSP00000360761.2:n.589-37_589-36del
ENST00000472820.1:n.517-37_517-36del
ENST00000538402.1:c.589-37_589-36del	ENSP00000438919.1:n.589-37_589-36del
NM_001012727.1:c.493-37_493-36del	NP_001012745.1:n.493-37_493-36del
NM_006412.3:c.589-37_589-36del	NP_006403.2:n.589-37_589-36del
NM_006412.4:c.589-37_589-36del MANE Select	NP_006403.2:n.589-37_589-36del
NM_001012727.2:c.493-37_493-36del	NP_001012745.1:n.493-37_493-36del