Canonical Allele Identifier: CA591186738

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1487778172
• gnomAD v2: 9-139581457-CT-C
• gnomAD v3: 9-136687005-CT-C
• gnomAD v4: 9-136687005-CT-C
• MyVariant Identifiers: chr9:g.139581458del (hg19) ; chr9:g.136687006del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136687006del , CM000671.2:g.136687006del	GRCh38
NC_000009.11:g.139581458del , CM000671.1:g.139581458del	GRCh37
NC_000009.10:g.138701279del	NCBI36
NG_008090.1:g.5454del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.182+170del MANE Select	ENSP00000360761.2:n.182+170del
ENST00000371694.7:c.182+170del	ENSP00000360759.3:n.182+170del
ENST00000371696.6:c.182+170del	ENSP00000360761.2:n.182+170del
ENST00000470861.1:n.190+170del
ENST00000538402.1:c.182+170del	ENSP00000438919.1:n.182+170del
NM_001012727.1:c.182+170del	NP_001012745.1:n.182+170del
NM_006412.3:c.182+170del	NP_006403.2:n.182+170del
NM_006412.4:c.182+170del MANE Select	NP_006403.2:n.182+170del
NM_001012727.2:c.182+170del	NP_001012745.1:n.182+170del