Canonical Allele Identifier: CA2692654701

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136676838-C-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676838C>T , CM000671.2:g.136676838C>T	GRCh38
NC_000009.11:g.139571290C>T , CM000671.1:g.139571290C>T	GRCh37
NC_000009.10:g.138691111C>T	NCBI36
NG_008090.1:g.15622G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+123G>A MANE Select	ENSP00000360761.2:n.492+123G>A
ENST00000371694.7:c.492+123G>A	ENSP00000360759.3:n.492+123G>A
ENST00000371696.6:c.492+123G>A	ENSP00000360761.2:n.492+123G>A
ENST00000472820.1:n.420+123G>A
ENST00000538402.1:c.492+123G>A	ENSP00000438919.1:n.492+123G>A
NM_001012727.1:c.492+123G>A	NP_001012745.1:n.492+123G>A
NM_006412.3:c.492+123G>A	NP_006403.2:n.492+123G>A
NM_006412.4:c.492+123G>A MANE Select	NP_006403.2:n.492+123G>A
NM_001012727.2:c.492+123G>A	NP_001012745.1:n.492+123G>A