Canonical Allele Identifier: CA2497275637

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1846229703

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136686990_136686997del , CM000671.2:g.136686990_136686997del	GRCh38
NC_000009.11:g.139581442_139581449del , CM000671.1:g.139581442_139581449del	GRCh37
NC_000009.10:g.138701263_138701270del	NCBI36
NG_008090.1:g.5466_5473del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.182+182_182+189del MANE Select	ENSP00000360761.2:n.182+182_182+189del
ENST00000371694.7:c.182+182_182+189del	ENSP00000360759.3:n.182+182_182+189del
ENST00000371696.6:c.182+182_182+189del	ENSP00000360761.2:n.182+182_182+189del
ENST00000470861.1:n.190+182_190+189del
ENST00000538402.1:c.182+182_182+189del	ENSP00000438919.1:n.182+182_182+189del
NM_001012727.1:c.182+182_182+189del	NP_001012745.1:n.182+182_182+189del
NM_006412.3:c.182+182_182+189del	NP_006403.2:n.182+182_182+189del
NM_006412.4:c.182+182_182+189del MANE Select	NP_006403.2:n.182+182_182+189del
NM_001012727.2:c.182+182_182+189del	NP_001012745.1:n.182+182_182+189del