Canonical Allele Identifier: CA379562836
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090142G>C , CM000673.2:g.8090142G>C GRCh38
NC_000011.9:g.8111689G>C , CM000673.1:g.8111689G>C GRCh37
NC_000011.8:g.8068265G>C NCBI36
NG_029912.1:g.56510G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.164G>C MANE Select ENSP00000299506.3:p.Arg55Pro
ENST00000299506.2:c.164G>C ENSP00000299506.2:p.Arg55Pro
ENST00000305253.8:c.329G>C ENSP00000305426.4:p.Arg110Pro
ENST00000534099.5:c.182G>C ENSP00000434400.1:p.Arg61Pro
NM_003320.4:c.329G>C NP_003311.2:p.Arg110Pro
NM_177972.2:c.164G>C NP_813977.1:p.Arg55Pro
XM_005253109.2:c.290G>C XP_005253166.1:p.Arg97Pro
XM_011520344.1:c.200G>C XP_011518646.1:p.Arg67Pro
XM_005253109.3:c.290G>C XP_005253166.1:p.Arg97Pro
XM_011520344.2:c.200G>C XP_011518646.1:p.Arg67Pro
NM_177972.3:c.164G>C MANE Select NP_813977.1:p.Arg55Pro
NM_003320.5:c.329G>C NP_003311.2:p.Arg110Pro