Canonical Allele Identifier: CA2692654610

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136676729-G-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676729G>C , CM000671.2:g.136676729G>C	GRCh38
NC_000009.11:g.139571181G>C , CM000671.1:g.139571181G>C	GRCh37
NC_000009.10:g.138691002G>C	NCBI36
NG_008090.1:g.15731C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.493-49C>G MANE Select	ENSP00000360761.2:n.493-49C>G
ENST00000371694.7:c.492+232C>G	ENSP00000360759.3:n.492+232C>G
ENST00000371696.6:c.493-49C>G	ENSP00000360761.2:n.493-49C>G
ENST00000472820.1:n.421-49C>G
ENST00000538402.1:c.493-49C>G	ENSP00000438919.1:n.493-49C>G
NM_001012727.1:c.492+232C>G	NP_001012745.1:n.492+232C>G
NM_006412.3:c.493-49C>G	NP_006403.2:n.493-49C>G
NM_006412.4:c.493-49C>G MANE Select	NP_006403.2:n.493-49C>G
NM_001012727.2:c.492+232C>G	NP_001012745.1:n.492+232C>G