Canonical Allele Identifier: CA2692654850
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

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