Canonical Allele Identifier: CA2720909548

Gene: AGPAT2

Linked Data

• dbSNP Id: rs2131023903

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687312_136687313insAAG , CM000671.2:g.136687312_136687313insAAG	GRCh38
NC_000009.11:g.139581764_139581765insAAG , CM000671.1:g.139581764_139581765insAAG	GRCh37
NC_000009.10:g.138701585_138701586insAAG	NCBI36
NG_008090.1:g.5149_5150insTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.47_48insTCT MANE Select	ENSP00000360761.2:p.Leu16_Leu17insLeu
ENST00000371694.7:c.47_48insTCT	ENSP00000360759.3:p.Leu16_Leu17insLeu
ENST00000371696.6:c.47_48insTCT	ENSP00000360761.2:p.Leu16_Leu17insLeu
ENST00000470861.1:n.55_56insTCT
ENST00000538402.1:c.47_48insTCT	ENSP00000438919.1:p.Leu16_Leu17insLeu
NM_001012727.1:c.47_48insTCT	NP_001012745.1:p.Leu16_Leu17insLeu
NM_006412.3:c.47_48insTCT	NP_006403.2:p.Leu16_Leu17insLeu
NM_006412.4:c.47_48insTCT MANE Select	NP_006403.2:p.Leu16_Leu17insLeu
NM_001012727.2:c.47_48insTCT	NP_001012745.1:p.Leu16_Leu17insLeu