Canonical Allele Identifier: CA2497275500

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1846039201

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136673556_136673583del , CM000671.2:g.136673556_136673583del	GRCh38
NC_000009.11:g.139568008_139568035del , CM000671.1:g.139568008_139568035del	GRCh37
NC_000009.10:g.138687829_138687856del	NCBI36
NG_008090.1:g.18879_18906del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.*171_*198del MANE Select	ENSP00000360761.2:n.*171_*198del
ENST00000371694.7:c.*171_*198del	ENSP00000360759.3:n.*171_*198del
ENST00000371696.6:c.*171_*198del	ENSP00000360761.2:n.*171_*198del
ENST00000538402.1:c.*171_*198del	ENSP00000438919.1:n.*171_*198del
NM_001012727.1:c.*171_*198del	NP_001012745.1:n.*171_*198del
NM_006412.3:c.*171_*198del	NP_006403.2:n.*171_*198del
NM_006412.4:c.*171_*198del MANE Select	NP_006403.2:n.*171_*198del
NM_001012727.2:c.*171_*198del	NP_001012745.1:n.*171_*198del