Canonical Allele Identifier: CA1130032883

Gene: AGPAT2

Linked Data

• gnomAD v3: 9-136673529-T-TGCCCTCGA
• gnomAD v4: 9-136673529-T-TGCCCTCGA

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673534_136673541dup , CM000671.2:g.136673534_136673541dup	GRCh38
NC_000009.11:g.139567986_139567993dup , CM000671.1:g.139567986_139567993dup	GRCh37
NC_000009.10:g.138687807_138687814dup	NCBI36
NG_008090.1:g.18923_18930dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.*215_*222dup MANE Select	ENSP00000360761.2:n.*215_*222dup
ENST00000371694.7:c.*215_*222dup	ENSP00000360759.3:n.*215_*222dup
ENST00000371696.6:c.*215_*222dup	ENSP00000360761.2:n.*215_*222dup
ENST00000538402.1:c.*215_*222dup	ENSP00000438919.1:n.*215_*222dup
NM_001012727.1:c.*215_*222dup	NP_001012745.1:n.*215_*222dup
NM_006412.3:c.*215_*222dup	NP_006403.2:n.*215_*222dup
NM_006412.4:c.*215_*222dup MANE Select	NP_006403.2:n.*215_*222dup
NM_001012727.2:c.*215_*222dup	NP_001012745.1:n.*215_*222dup