Canonical Allele Identifier: CA2579519916

Gene: AGPAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674705_136674710del , CM000671.2:g.136674705_136674710del	GRCh38
NC_000009.11:g.139569157_139569162del , CM000671.1:g.139569157_139569162del	GRCh37
NC_000009.10:g.138688978_138688983del	NCBI36
NG_008090.1:g.17752_17757del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.661+27_661+32del MANE Select	ENSP00000360761.2:n.661+27_661+32del
ENST00000371694.7:c.565+27_565+32del	ENSP00000360759.3:n.565+27_565+32del
ENST00000371696.6:c.661+27_661+32del	ENSP00000360761.2:n.661+27_661+32del
ENST00000472820.1:n.589+27_589+32del
ENST00000538402.1:c.661+27_661+32del	ENSP00000438919.1:n.661+27_661+32del
NM_001012727.1:c.565+27_565+32del	NP_001012745.1:n.565+27_565+32del
NM_006412.3:c.661+27_661+32del	NP_006403.2:n.661+27_661+32del
NM_006412.4:c.661+27_661+32del MANE Select	NP_006403.2:n.661+27_661+32del
NM_001012727.2:c.565+27_565+32del	NP_001012745.1:n.565+27_565+32del