Canonical Allele Identifier: CA2692655338

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136687143-TCCCCGGCCCCTCCCGGCGGC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687152_136687171del , CM000671.2:g.136687152_136687171del	GRCh38
NC_000009.11:g.139581604_139581623del , CM000671.1:g.139581604_139581623del	GRCh37
NC_000009.10:g.138701425_138701444del	NCBI36
NG_008090.1:g.5297_5316del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.182+13_182+32del MANE Select	ENSP00000360761.2:n.182+13_182+32del
ENST00000371694.7:c.182+13_182+32del	ENSP00000360759.3:n.182+13_182+32del
ENST00000371696.6:c.182+13_182+32del	ENSP00000360761.2:n.182+13_182+32del
ENST00000470861.1:n.190+13_190+32del
ENST00000538402.1:c.182+13_182+32del	ENSP00000438919.1:n.182+13_182+32del
NM_001012727.1:c.182+13_182+32del	NP_001012745.1:n.182+13_182+32del
NM_006412.3:c.182+13_182+32del	NP_006403.2:n.182+13_182+32del
NM_006412.4:c.182+13_182+32del MANE Select	NP_006403.2:n.182+13_182+32del
NM_001012727.2:c.182+13_182+32del	NP_001012745.1:n.182+13_182+32del