Canonical Allele Identifier: CA2497275519

Gene: AGPAT2

Linked Data

• dbSNP Id: rs1846069579

Genomic Alleles

HGVS	Genome Assembly
NC_000009.12:g.136674812_136674863del , CM000671.2:g.136674812_136674863del	GRCh38
NC_000009.11:g.139569264_139569315del , CM000671.1:g.139569264_139569315del	GRCh37
NC_000009.10:g.138689085_138689136del	NCBI36
NG_008090.1:g.17598_17649del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000371696.7:c.589-55_589-4del MANE Select	ENSP00000360761.2:n.589-55_589-4del
ENST00000371694.7:c.493-55_493-4del	ENSP00000360759.3:n.493-55_493-4del
ENST00000371696.6:c.589-55_589-4del	ENSP00000360761.2:n.589-55_589-4del
ENST00000472820.1:n.517-55_517-4del
ENST00000538402.1:c.589-55_589-4del	ENSP00000438919.1:n.589-55_589-4del
NM_001012727.1:c.493-55_493-4del	NP_001012745.1:n.493-55_493-4del
NM_006412.3:c.589-55_589-4del	NP_006403.2:n.589-55_589-4del
NM_006412.4:c.589-55_589-4del MANE Select	NP_006403.2:n.589-55_589-4del
NM_001012727.2:c.493-55_493-4del	NP_001012745.1:n.493-55_493-4del