Canonical Allele Identifier: CA1130033678
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674662_136674673dup , CM000671.2:g.136674662_136674673dup GRCh38
NC_000009.11:g.139569114_139569125dup , CM000671.1:g.139569114_139569125dup GRCh37
NC_000009.10:g.138688935_138688946dup NCBI36
NG_008090.1:g.17789_17800dup

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.661+64_661+75dup MANE Select ENSP00000360761.2:n.661+64_661+75dup
ENST00000371694.7:c.565+64_565+75dup ENSP00000360759.3:n.565+64_565+75dup
ENST00000371696.6:c.661+64_661+75dup ENSP00000360761.2:n.661+64_661+75dup
ENST00000472820.1:n.589+64_589+75dup
ENST00000538402.1:c.661+64_661+75dup ENSP00000438919.1:n.661+64_661+75dup
NM_001012727.1:c.565+64_565+75dup NP_001012745.1:n.565+64_565+75dup
NM_006412.3:c.661+64_661+75dup NP_006403.2:n.661+64_661+75dup
NM_006412.4:c.661+64_661+75dup MANE Select NP_006403.2:n.661+64_661+75dup
NM_001012727.2:c.565+64_565+75dup NP_001012745.1:n.565+64_565+75dup