Canonical Allele Identifier: CA2193053007
Gene: AGBL1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.86117552T= , CM000677.2:g.86117552T= GRCh38
NC_000015.9:g.86660783T= , CM000677.1:g.86660783T= GRCh37
NC_000015.8:g.84461787T= NCBI36
NG_033836.2:g.42745T=

Transcript Alleles

HGVS Amino-acid change
ENST00000441037.7:c.52-24452T= ENSP00000413001.3:n.52-24452T=
ENST00000614907.3:c.52-24452T= MANE Select ENSP00000490608.2:n.52-24452T=
XM_011521226.1:c.52-24452T= XP_011519528.1:n.52-24452T=
XM_011521227.1:c.52-24452T= XP_011519529.1:n.52-24452T=
XM_011521228.1:c.52-24452T= XP_011519530.1:n.52-24452T=
XM_011521229.1:c.52-24452T= XP_011519531.1:n.52-24452T=
XM_011521230.1:c.52-24452T= XP_011519532.1:n.52-24452T=
XR_931750.1:n.238-24452T=
XR_931751.1:n.238-24452T=
NM_152336.3:c.52-24452T= NP_689549.3:n.52-24452T=
XM_011521226.3:c.52-24452T= XP_011519528.1:n.52-24452T=
XM_011521227.3:c.52-24452T= XP_011519529.1:n.52-24452T=
XM_011521228.3:c.52-24452T= XP_011519530.1:n.52-24452T=
XM_011521230.3:c.52-24452T= XP_011519532.1:n.52-24452T=
XM_017021918.2:c.52-24452T= XP_016877407.1:n.52-24452T=
XM_017021919.2:c.52-24452T= XP_016877408.1:n.52-24452T=
XM_017021920.2:c.52-24452T= XP_016877409.1:n.52-24452T=
XM_017021921.2:c.52-24452T= XP_016877410.1:n.52-24452T=
XR_931750.3:n.386-24452T=
XR_931751.3:n.386-24452T=
NM_152336.4:c.52-24452T= NP_689549.3:n.52-24452T=
NM_001386094.1:c.52-24452T= MANE Select NP_001373023.1:n.52-24452T=