Canonical Allele Identifier: CA2695211767

Gene: AGPAT2

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687283_136687284insAA , CM000671.2:g.136687283_136687284insAA	GRCh38
NC_000009.11:g.139581735_139581736insAA , CM000671.1:g.139581735_139581736insAA	GRCh37
NC_000009.10:g.138701556_138701557insAA	NCBI36
NG_008090.1:g.5176_5177insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.74_75insTT MANE Select	ENSP00000360761.2:p.Glu25AspfsTer?
ENST00000371694.7:c.74_75insTT	ENSP00000360759.3:p.Glu25AspfsTer?
ENST00000371696.6:c.74_75insTT	ENSP00000360761.2:p.Glu25AspfsTer?
ENST00000470861.1:n.82_83insTT
ENST00000538402.1:c.74_75insTT	ENSP00000438919.1:p.Glu25AspfsTer?
NM_001012727.1:c.74_75insTT	NP_001012745.1:p.Glu25AspfsTer?
NM_006412.3:c.74_75insTT	NP_006403.2:p.Glu25AspfsTer?
NM_006412.4:c.74_75insTT MANE Select	NP_006403.2:p.Glu25AspfsTer?
NM_001012727.2:c.74_75insTT	NP_001012745.1:p.Glu25AspfsTer?