Canonical Allele Identifier: CA2786279659

Gene: AGPAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687108_136687109del , CM000671.2:g.136687108_136687109del	GRCh38
NC_000009.11:g.139581560_139581561del , CM000671.1:g.139581560_139581561del	GRCh37
NC_000009.10:g.138701381_138701382del	NCBI36
NG_008090.1:g.5352_5353del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.182+68_182+69del MANE Select	ENSP00000360761.2:n.182+68_182+69del
ENST00000371694.7:c.182+68_182+69del	ENSP00000360759.3:n.182+68_182+69del
ENST00000371696.6:c.182+68_182+69del	ENSP00000360761.2:n.182+68_182+69del
ENST00000470861.1:n.190+68_190+69del
ENST00000538402.1:c.182+68_182+69del	ENSP00000438919.1:n.182+68_182+69del
NM_001012727.1:c.182+68_182+69del	NP_001012745.1:n.182+68_182+69del
NM_006412.3:c.182+68_182+69del	NP_006403.2:n.182+68_182+69del
NM_006412.4:c.182+68_182+69del MANE Select	NP_006403.2:n.182+68_182+69del
NM_001012727.2:c.182+68_182+69del	NP_001012745.1:n.182+68_182+69del