Canonical Allele Identifier: CA2692654698

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136676836-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676836A>G , CM000671.2:g.136676836A>G	GRCh38
NC_000009.11:g.139571288A>G , CM000671.1:g.139571288A>G	GRCh37
NC_000009.10:g.138691109A>G	NCBI36
NG_008090.1:g.15624T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+125T>C MANE Select	ENSP00000360761.2:n.492+125T>C
ENST00000371694.7:c.492+125T>C	ENSP00000360759.3:n.492+125T>C
ENST00000371696.6:c.492+125T>C	ENSP00000360761.2:n.492+125T>C
ENST00000472820.1:n.420+125T>C
ENST00000538402.1:c.492+125T>C	ENSP00000438919.1:n.492+125T>C
NM_001012727.1:c.492+125T>C	NP_001012745.1:n.492+125T>C
NM_006412.3:c.492+125T>C	NP_006403.2:n.492+125T>C
NM_006412.4:c.492+125T>C MANE Select	NP_006403.2:n.492+125T>C
NM_001012727.2:c.492+125T>C	NP_001012745.1:n.492+125T>C