Canonical Allele Identifier: CA2692653722

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136673733-T-TGG

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673734_136673735insGG , CM000671.2:g.136673734_136673735insGG	GRCh38
NC_000009.11:g.139568186_139568187insGG , CM000671.1:g.139568186_139568187insGG	GRCh37
NC_000009.10:g.138688007_138688008insGG	NCBI36
NG_008090.1:g.18726_18727insCC

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.*18_*19insCC MANE Select	ENSP00000360761.2:n.*18_*19insCC
ENST00000371694.7:c.*18_*19insCC	ENSP00000360759.3:n.*18_*19insCC
ENST00000371696.6:c.*18_*19insCC	ENSP00000360761.2:n.*18_*19insCC
ENST00000472820.1:n.783_784insCC
ENST00000538402.1:c.*18_*19insCC	ENSP00000438919.1:n.*18_*19insCC
NM_001012727.1:c.*18_*19insCC	NP_001012745.1:n.*18_*19insCC
NM_006412.3:c.*18_*19insCC	NP_006403.2:n.*18_*19insCC
NM_006412.4:c.*18_*19insCC MANE Select	NP_006403.2:n.*18_*19insCC
NM_001012727.2:c.*18_*19insCC	NP_001012745.1:n.*18_*19insCC