Canonical Allele Identifier: CA2692654189
Gene: AGPAT2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000009.12:g.136674711_136674712dup , CM000671.2:g.136674711_136674712dup GRCh38
NC_000009.11:g.139569163_139569164dup , CM000671.1:g.139569163_139569164dup GRCh37
NC_000009.10:g.138688984_138688985dup NCBI36
NG_008090.1:g.17750_17751dup

Transcript Alleles

HGVS Amino-acid change
ENST00000371696.7:c.661+25_661+26dup MANE Select ENSP00000360761.2:n.661+25_661+26dup
ENST00000371694.7:c.565+25_565+26dup ENSP00000360759.3:n.565+25_565+26dup
ENST00000371696.6:c.661+25_661+26dup ENSP00000360761.2:n.661+25_661+26dup
ENST00000472820.1:n.589+25_589+26dup
ENST00000538402.1:c.661+25_661+26dup ENSP00000438919.1:n.661+25_661+26dup
NM_001012727.1:c.565+25_565+26dup NP_001012745.1:n.565+25_565+26dup
NM_006412.3:c.661+25_661+26dup NP_006403.2:n.661+25_661+26dup
NM_006412.4:c.661+25_661+26dup MANE Select NP_006403.2:n.661+25_661+26dup
NM_001012727.2:c.565+25_565+26dup NP_001012745.1:n.565+25_565+26dup