Canonical Allele Identifier: CA379562755
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090123C>A , CM000673.2:g.8090123C>A GRCh38
NC_000011.9:g.8111670C>A , CM000673.1:g.8111670C>A GRCh37
NC_000011.8:g.8068246C>A NCBI36
NG_029912.1:g.56491C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.145C>A MANE Select ENSP00000299506.3:p.Gln49Lys
ENST00000299506.2:c.145C>A ENSP00000299506.2:p.Gln49Lys
ENST00000305253.8:c.310C>A ENSP00000305426.4:p.Gln104Lys
ENST00000534099.5:c.163C>A ENSP00000434400.1:p.Gln55Lys
NM_003320.4:c.310C>A NP_003311.2:p.Gln104Lys
NM_177972.2:c.145C>A NP_813977.1:p.Gln49Lys
XM_005253109.2:c.271C>A XP_005253166.1:p.Gln91Lys
XM_011520344.1:c.181C>A XP_011518646.1:p.Gln61Lys
XM_005253109.3:c.271C>A XP_005253166.1:p.Gln91Lys
XM_011520344.2:c.181C>A XP_011518646.1:p.Gln61Lys
NM_177972.3:c.145C>A MANE Select NP_813977.1:p.Gln49Lys
NM_003320.5:c.310C>A NP_003311.2:p.Gln104Lys