Canonical Allele Identifier: CA2497275497

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1846038625

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673537_136673543del , CM000671.2:g.136673537_136673543del	GRCh38
NC_000009.11:g.139567989_139567995del , CM000671.1:g.139567989_139567995del	GRCh37
NC_000009.10:g.138687810_138687816del	NCBI36
NG_008090.1:g.18918_18924del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.*210_*216del MANE Select	ENSP00000360761.2:n.*210_*216del
ENST00000371694.7:c.*210_*216del	ENSP00000360759.3:n.*210_*216del
ENST00000371696.6:c.*210_*216del	ENSP00000360761.2:n.*210_*216del
ENST00000538402.1:c.*210_*216del	ENSP00000438919.1:n.*210_*216del
NM_001012727.1:c.*210_*216del	NP_001012745.1:n.*210_*216del
NM_006412.3:c.*210_*216del	NP_006403.2:n.*210_*216del
NM_006412.4:c.*210_*216del MANE Select	NP_006403.2:n.*210_*216del
NM_001012727.2:c.*210_*216del	NP_001012745.1:n.*210_*216del