Canonical Allele Identifier: CA1130033011

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1846043547
• gnomAD v3: 9-136673739-GCC-G
• gnomAD v4: 9-136673739-GCC-G

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673740_136673741del , CM000671.2:g.136673740_136673741del	GRCh38
NC_000009.11:g.139568192_139568193del , CM000671.1:g.139568192_139568193del	GRCh37
NC_000009.10:g.138688013_138688014del	NCBI36
NG_008090.1:g.18719_18720del

Transcript Alleles

HGVS	Amino-acid change
ENST00000371696.7:c.*11_*12del MANE Select	ENSP00000360761.2:n.*11_*12del
ENST00000371694.7:c.*11_*12del	ENSP00000360759.3:n.*11_*12del
ENST00000371696.6:c.*11_*12del	ENSP00000360761.2:n.*11_*12del
ENST00000472820.1:n.776_777del
ENST00000538402.1:c.*11_*12del	ENSP00000438919.1:n.*11_*12del
NM_001012727.1:c.*11_*12del	NP_001012745.1:n.*11_*12del
NM_006412.3:c.*11_*12del	NP_006403.2:n.*11_*12del
NM_006412.4:c.*11_*12del MANE Select	NP_006403.2:n.*11_*12del
NM_001012727.2:c.*11_*12del	NP_001012745.1:n.*11_*12del