Canonical Allele Identifier: CA379562326
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089630G>A , CM000673.2:g.8089630G>A GRCh38
NC_000011.9:g.8111177G>A , CM000673.1:g.8111177G>A GRCh37
NC_000011.8:g.8067753G>A NCBI36
NG_029912.1:g.55998G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.59G>A MANE Select ENSP00000299506.3:p.Arg20Lys
ENST00000299506.2:c.59G>A ENSP00000299506.2:p.Arg20Lys
ENST00000305253.8:c.224G>A ENSP00000305426.4:p.Arg75Lys
ENST00000534099.5:c.77G>A ENSP00000434400.1:p.Arg26Lys
NM_003320.4:c.224G>A NP_003311.2:p.Arg75Lys
NM_177972.2:c.59G>A NP_813977.1:p.Arg20Lys
XM_005253109.2:c.185G>A XP_005253166.1:p.Arg62Lys
XM_011520344.1:c.95G>A XP_011518646.1:p.Arg32Lys
XM_005253109.3:c.185G>A XP_005253166.1:p.Arg62Lys
XM_011520344.2:c.95G>A XP_011518646.1:p.Arg32Lys
NM_177972.3:c.59G>A MANE Select NP_813977.1:p.Arg20Lys
NM_003320.5:c.224G>A NP_003311.2:p.Arg75Lys