Canonical Allele Identifier: CA2692654697

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136676835-C-CT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676835_136676836insT , CM000671.2:g.136676835_136676836insT	GRCh38
NC_000009.11:g.139571287_139571288insT , CM000671.1:g.139571287_139571288insT	GRCh37
NC_000009.10:g.138691108_138691109insT	NCBI36
NG_008090.1:g.15624_15625insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+125_492+126insA MANE Select	ENSP00000360761.2:n.492+125_492+126insA
ENST00000371694.7:c.492+125_492+126insA	ENSP00000360759.3:n.492+125_492+126insA
ENST00000371696.6:c.492+125_492+126insA	ENSP00000360761.2:n.492+125_492+126insA
ENST00000472820.1:n.420+125_420+126insA
ENST00000538402.1:c.492+125_492+126insA	ENSP00000438919.1:n.492+125_492+126insA
NM_001012727.1:c.492+125_492+126insA	NP_001012745.1:n.492+125_492+126insA
NM_006412.3:c.492+125_492+126insA	NP_006403.2:n.492+125_492+126insA
NM_006412.4:c.492+125_492+126insA MANE Select	NP_006403.2:n.492+125_492+126insA
NM_001012727.2:c.492+125_492+126insA	NP_001012745.1:n.492+125_492+126insA