Canonical Allele Identifier: CA2692654760
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136676898del , CM000671.2:g.136676898del GRCh38
NC_000009.11:g.139571350del , CM000671.1:g.139571350del GRCh37
NC_000009.10:g.138691171del NCBI36
NG_008090.1:g.15563del

Transcript Alleles

HGVS Amino-acid Change
ENST00000371696.7:c.492+64del MANE Select ENSP00000360761.2:n.492+64del
ENST00000371694.7:c.492+64del ENSP00000360759.3:n.492+64del
ENST00000371696.6:c.492+64del ENSP00000360761.2:n.492+64del
ENST00000472820.1:n.420+64del
ENST00000538402.1:c.492+64del ENSP00000438919.1:n.492+64del
NM_001012727.1:c.492+64del NP_001012745.1:n.492+64del
NM_006412.3:c.492+64del NP_006403.2:n.492+64del
NM_006412.4:c.492+64del MANE Select NP_006403.2:n.492+64del
NM_001012727.2:c.492+64del NP_001012745.1:n.492+64del