Canonical Allele Identifier: CA2692654324
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674868_136674869insACA , CM000671.2:g.136674868_136674869insACA GRCh38
NC_000009.11:g.139569320_139569321insACA , CM000671.1:g.139569320_139569321insACA GRCh37
NC_000009.10:g.138689141_138689142insACA NCBI36
NG_008090.1:g.17591_17592insTGT

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.589-62_589-61insTGT MANE Select ENSP00000360761.2:n.589-62_589-61insTGT
ENST00000371694.7:c.493-62_493-61insTGT ENSP00000360759.3:n.493-62_493-61insTGT
ENST00000371696.6:c.589-62_589-61insTGT ENSP00000360761.2:n.589-62_589-61insTGT
ENST00000472820.1:n.517-62_517-61insTGT
ENST00000538402.1:c.589-62_589-61insTGT ENSP00000438919.1:n.589-62_589-61insTGT
NM_001012727.1:c.493-62_493-61insTGT NP_001012745.1:n.493-62_493-61insTGT
NM_006412.3:c.589-62_589-61insTGT NP_006403.2:n.589-62_589-61insTGT
NM_006412.4:c.589-62_589-61insTGT MANE Select NP_006403.2:n.589-62_589-61insTGT
NM_001012727.2:c.493-62_493-61insTGT NP_001012745.1:n.493-62_493-61insTGT