Canonical Allele Identifier: CA2579519976

Gene: AGPAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676693_136676695del , CM000671.2:g.136676693_136676695del	GRCh38
NC_000009.11:g.139571145_139571147del , CM000671.1:g.139571145_139571147del	GRCh37
NC_000009.10:g.138690966_138690968del	NCBI36
NG_008090.1:g.15768_15770del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.493-12_493-10del MANE Select	ENSP00000360761.2:n.493-12_493-10del
ENST00000371694.7:c.492+269_492+271del	ENSP00000360759.3:n.492+269_492+271del
ENST00000371696.6:c.493-12_493-10del	ENSP00000360761.2:n.493-12_493-10del
ENST00000472820.1:n.421-12_421-10del
ENST00000538402.1:c.493-12_493-10del	ENSP00000438919.1:n.493-12_493-10del
NM_001012727.1:c.492+269_492+271del	NP_001012745.1:n.492+269_492+271del
NM_006412.3:c.493-12_493-10del	NP_006403.2:n.493-12_493-10del
NM_006412.4:c.493-12_493-10del MANE Select	NP_006403.2:n.493-12_493-10del
NM_001012727.2:c.492+269_492+271del	NP_001012745.1:n.492+269_492+271del