Canonical Allele Identifier: CA2497275520

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1846070888

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674907_136674908insA , CM000671.2:g.136674907_136674908insA	GRCh38
NC_000009.11:g.139569359_139569360insA , CM000671.1:g.139569359_139569360insA	GRCh37
NC_000009.10:g.138689180_138689181insA	NCBI36
NG_008090.1:g.17552_17553insT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.589-101_589-100insT MANE Select	ENSP00000360761.2:n.589-101_589-100insT
ENST00000371694.7:c.493-101_493-100insT	ENSP00000360759.3:n.493-101_493-100insT
ENST00000371696.6:c.589-101_589-100insT	ENSP00000360761.2:n.589-101_589-100insT
ENST00000472820.1:n.517-101_517-100insT
ENST00000538402.1:c.589-101_589-100insT	ENSP00000438919.1:n.589-101_589-100insT
NM_001012727.1:c.493-101_493-100insT	NP_001012745.1:n.493-101_493-100insT
NM_006412.3:c.589-101_589-100insT	NP_006403.2:n.589-101_589-100insT
NM_006412.4:c.589-101_589-100insT MANE Select	NP_006403.2:n.589-101_589-100insT
NM_001012727.2:c.493-101_493-100insT	NP_001012745.1:n.493-101_493-100insT