Canonical Allele Identifier: CA2692654035

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674621-C-CA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674621_136674622insA , CM000671.2:g.136674621_136674622insA	GRCh38
NC_000009.11:g.139569073_139569074insA , CM000671.1:g.139569073_139569074insA	GRCh37
NC_000009.10:g.138688894_138688895insA	NCBI36
NG_008090.1:g.17838_17839insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.661+113_661+114insT MANE Select	ENSP00000360761.2:n.661+113_661+114insT
ENST00000371694.7:c.565+113_565+114insT	ENSP00000360759.3:n.565+113_565+114insT
ENST00000371696.6:c.661+113_661+114insT	ENSP00000360761.2:n.661+113_661+114insT
ENST00000472820.1:n.589+113_589+114insT
ENST00000538402.1:c.661+113_661+114insT	ENSP00000438919.1:n.661+113_661+114insT
NM_001012727.1:c.565+113_565+114insT	NP_001012745.1:n.565+113_565+114insT
NM_006412.3:c.661+113_661+114insT	NP_006403.2:n.661+113_661+114insT
NM_006412.4:c.661+113_661+114insT MANE Select	NP_006403.2:n.661+113_661+114insT
NM_001012727.2:c.565+113_565+114insT	NP_001012745.1:n.565+113_565+114insT