Canonical Allele Identifier: CA2692654126

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136674667-G-GGGC

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674668_136674670dup , CM000671.2:g.136674668_136674670dup	GRCh38
NC_000009.11:g.139569120_139569122dup , CM000671.1:g.139569120_139569122dup	GRCh37
NC_000009.10:g.138688941_138688943dup	NCBI36
NG_008090.1:g.17790_17792dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.661+65_661+67dup MANE Select	ENSP00000360761.2:n.661+65_661+67dup
ENST00000371694.7:c.565+65_565+67dup	ENSP00000360759.3:n.565+65_565+67dup
ENST00000371696.6:c.661+65_661+67dup	ENSP00000360761.2:n.661+65_661+67dup
ENST00000472820.1:n.589+65_589+67dup
ENST00000538402.1:c.661+65_661+67dup	ENSP00000438919.1:n.661+65_661+67dup
NM_001012727.1:c.565+65_565+67dup	NP_001012745.1:n.565+65_565+67dup
NM_006412.3:c.661+65_661+67dup	NP_006403.2:n.661+65_661+67dup
NM_006412.4:c.661+65_661+67dup MANE Select	NP_006403.2:n.661+65_661+67dup
NM_001012727.2:c.565+65_565+67dup	NP_001012745.1:n.565+65_565+67dup