Canonical Allele Identifier: CA379562263
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089617G>T , CM000673.2:g.8089617G>T GRCh38
NC_000011.9:g.8111164G>T , CM000673.1:g.8111164G>T GRCh37
NC_000011.8:g.8067740G>T NCBI36
NG_029912.1:g.55985G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.46G>T MANE Select ENSP00000299506.3:p.Asp16Tyr
ENST00000299506.2:c.46G>T ENSP00000299506.2:p.Asp16Tyr
ENST00000305253.8:c.211G>T ENSP00000305426.4:p.Asp71Tyr
ENST00000534099.5:c.64G>T ENSP00000434400.1:p.Asp22Tyr
NM_003320.4:c.211G>T NP_003311.2:p.Asp71Tyr
NM_177972.2:c.46G>T NP_813977.1:p.Asp16Tyr
XM_005253109.2:c.172G>T XP_005253166.1:p.Asp58Tyr
XM_011520344.1:c.82G>T XP_011518646.1:p.Asp28Tyr
XM_005253109.3:c.172G>T XP_005253166.1:p.Asp58Tyr
XM_011520344.2:c.82G>T XP_011518646.1:p.Asp28Tyr
NM_177972.3:c.46G>T MANE Select NP_813977.1:p.Asp16Tyr
NM_003320.5:c.211G>T NP_003311.2:p.Asp71Tyr