Canonical Allele Identifier: CA379562787
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090130A>C , CM000673.2:g.8090130A>C GRCh38
NC_000011.9:g.8111677A>C , CM000673.1:g.8111677A>C GRCh37
NC_000011.8:g.8068253A>C NCBI36
NG_029912.1:g.56498A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.152A>C MANE Select ENSP00000299506.3:p.Asn51Thr
ENST00000299506.2:c.152A>C ENSP00000299506.2:p.Asn51Thr
ENST00000305253.8:c.317A>C ENSP00000305426.4:p.Asn106Thr
ENST00000534099.5:c.170A>C ENSP00000434400.1:p.Asn57Thr
NM_003320.4:c.317A>C NP_003311.2:p.Asn106Thr
NM_177972.2:c.152A>C NP_813977.1:p.Asn51Thr
XM_005253109.2:c.278A>C XP_005253166.1:p.Asn93Thr
XM_011520344.1:c.188A>C XP_011518646.1:p.Asn63Thr
XM_005253109.3:c.278A>C XP_005253166.1:p.Asn93Thr
XM_011520344.2:c.188A>C XP_011518646.1:p.Asn63Thr
NM_177972.3:c.152A>C MANE Select NP_813977.1:p.Asn51Thr
NM_003320.5:c.317A>C NP_003311.2:p.Asn106Thr