Canonical Allele Identifier: CA2692653417

Gene: AGPAT2

Linked Data

• gnomAD v4: 9-136673541-CGGGGAGGGTCCAGCT-C

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673543_136673557del , CM000671.2:g.136673543_136673557del	GRCh38
NC_000009.11:g.139567995_139568009del , CM000671.1:g.139567995_139568009del	GRCh37
NC_000009.10:g.138687816_138687830del	NCBI36
NG_008090.1:g.18904_18918del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.*196_*210del MANE Select	ENSP00000360761.2:n.*196_*210del
ENST00000371694.7:c.*196_*210del	ENSP00000360759.3:n.*196_*210del
ENST00000371696.6:c.*196_*210del	ENSP00000360761.2:n.*196_*210del
ENST00000538402.1:c.*196_*210del	ENSP00000438919.1:n.*196_*210del
NM_001012727.1:c.*196_*210del	NP_001012745.1:n.*196_*210del
NM_006412.3:c.*196_*210del	NP_006403.2:n.*196_*210del
NM_006412.4:c.*196_*210del MANE Select	NP_006403.2:n.*196_*210del
NM_001012727.2:c.*196_*210del	NP_001012745.1:n.*196_*210del