Canonical Allele Identifier: CA1130035600

Gene: AGPAT2

Linked Data

• gnomAD v3: 9-136676910-C-CACCCTGCCTTCT
• gnomAD v4: 9-136676910-C-CACCCTGCCTTCT

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136676910_136676911insACCCTGCCTTCT , CM000671.2:g.136676910_136676911insACCCTGCCTTCT	GRCh38
NC_000009.11:g.139571362_139571363insACCCTGCCTTCT , CM000671.1:g.139571362_139571363insACCCTGCCTTCT	GRCh37
NC_000009.10:g.138691183_138691184insACCCTGCCTTCT	NCBI36
NG_008090.1:g.15549_15550insAGAAGGCAGGGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.492+50_492+51insAGAAGGCAGGGT MANE Select	ENSP00000360761.2:n.492+50_492+51insAGAAGGCAGGGT
ENST00000371694.7:c.492+50_492+51insAGAAGGCAGGGT	ENSP00000360759.3:n.492+50_492+51insAGAAGGCAGGGT
ENST00000371696.6:c.492+50_492+51insAGAAGGCAGGGT	ENSP00000360761.2:n.492+50_492+51insAGAAGGCAGGGT
ENST00000472820.1:n.420+50_420+51insAGAAGGCAGGGT
ENST00000538402.1:c.492+50_492+51insAGAAGGCAGGGT	ENSP00000438919.1:n.492+50_492+51insAGAAGGCAGGGT
NM_001012727.1:c.492+50_492+51insAGAAGGCAGGGT	NP_001012745.1:n.492+50_492+51insAGAAGGCAGGGT
NM_006412.3:c.492+50_492+51insAGAAGGCAGGGT	NP_006403.2:n.492+50_492+51insAGAAGGCAGGGT
NM_006412.4:c.492+50_492+51insAGAAGGCAGGGT MANE Select	NP_006403.2:n.492+50_492+51insAGAAGGCAGGGT
NM_001012727.2:c.492+50_492+51insAGAAGGCAGGGT	NP_001012745.1:n.492+50_492+51insAGAAGGCAGGGT