Canonical Allele Identifier: CA2692655246

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136687068-AGCGGGGCGGGACGG-A

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687076_136687089del , CM000671.2:g.136687076_136687089del	GRCh38
NC_000009.11:g.139581528_139581541del , CM000671.1:g.139581528_139581541del	GRCh37
NC_000009.10:g.138701349_138701362del	NCBI36
NG_008090.1:g.5378_5391del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.182+94_182+107del MANE Select	ENSP00000360761.2:n.182+94_182+107del
ENST00000371694.7:c.182+94_182+107del	ENSP00000360759.3:n.182+94_182+107del
ENST00000371696.6:c.182+94_182+107del	ENSP00000360761.2:n.182+94_182+107del
ENST00000470861.1:n.190+94_190+107del
ENST00000538402.1:c.182+94_182+107del	ENSP00000438919.1:n.182+94_182+107del
NM_001012727.1:c.182+94_182+107del	NP_001012745.1:n.182+94_182+107del
NM_006412.3:c.182+94_182+107del	NP_006403.2:n.182+94_182+107del
NM_006412.4:c.182+94_182+107del MANE Select	NP_006403.2:n.182+94_182+107del
NM_001012727.2:c.182+94_182+107del	NP_001012745.1:n.182+94_182+107del