Canonical Allele Identifier: CA861082764
Gene: AGPAT2 HGNC NCBI

Linked Data

dbSNP Id: rs1323323190
MyVariant Identifiers: chr9:g.139571384del (hg19) chr9:g.136676932del (hg38)
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676935del , CM000671.2:g.136676935del GRCh38
NC_000009.11:g.139571387del , CM000671.1:g.139571387del GRCh37
NC_000009.10:g.138691208del NCBI36
NG_008090.1:g.15528del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.492+29del MANE Select ENSP00000360761.2:n.492+29del
ENST00000371694.7:c.492+29del ENSP00000360759.3:n.492+29del
ENST00000371696.6:c.492+29del ENSP00000360761.2:n.492+29del
ENST00000472820.1:n.420+29del
ENST00000538402.1:c.492+29del ENSP00000438919.1:n.492+29del
NM_001012727.1:c.492+29del NP_001012745.1:n.492+29del
NM_006412.3:c.492+29del NP_006403.2:n.492+29del
NM_006412.4:c.492+29del MANE Select NP_006403.2:n.492+29del
NM_001012727.2:c.492+29del NP_001012745.1:n.492+29del
Search 100 bp 5'
Search 100 bp 3'