Canonical Allele Identifier: CA274940548
Gene: AGBL1 HGNC NCBI

Linked Data

dbSNP Id: rs17647114

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.86893514G>A , CM000677.2:g.86893514G>A GRCh38
NC_000015.9:g.87436745G>A , CM000677.1:g.87436745G>A GRCh37
NC_000015.8:g.85237749G>A NCBI36
NG_033836.1:g.756504G>A
NG_033836.2:g.818707G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000441037.7:c.3222-94473G>A ENSP00000413001.3:n.3222-94473G>A
ENST00000614907.3:c.3159-13573G>A MANE Select ENSP00000490608.2:n.3159-13573G>A
ENST00000681381.1:n.318-148491G>A
ENST00000441037.6:c.3084-94473G>A ENSP00000413001.2:n.3084-94473G>A
NM_152336.2:c.3084-94473G>A NP_689549.2:n.3084-94473G>A
XM_011521226.1:c.3159-13573G>A XP_011519528.1:n.3159-13573G>A
XM_011521227.1:c.3159-135311G>A XP_011519529.1:n.3159-135311G>A
NM_152336.3:c.3222-94473G>A NP_689549.3:n.3222-94473G>A
XM_011521226.3:c.3159-13573G>A XP_011519528.1:n.3159-13573G>A
XM_011521227.3:c.3159-135311G>A XP_011519529.1:n.3159-135311G>A
XM_017021918.2:c.3126-13573G>A XP_016877407.1:n.3126-13573G>A
XM_017021919.2:c.3075-13573G>A XP_016877408.1:n.3075-13573G>A
NM_152336.4:c.3222-94473G>A NP_689549.3:n.3222-94473G>A
NM_001386094.1:c.3159-13573G>A MANE Select NP_001373023.1:n.3159-13573G>A