Canonical Allele Identifier: CA379562631
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090094A>C , CM000673.2:g.8090094A>C GRCh38
NC_000011.9:g.8111641A>C , CM000673.1:g.8111641A>C GRCh37
NC_000011.8:g.8068217A>C NCBI36
NG_029912.1:g.56462A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.116A>C MANE Select ENSP00000299506.3:p.Lys39Thr
ENST00000299506.2:c.116A>C ENSP00000299506.2:p.Lys39Thr
ENST00000305253.8:c.281A>C ENSP00000305426.4:p.Lys94Thr
ENST00000534099.5:c.134A>C ENSP00000434400.1:p.Lys45Thr
NM_003320.4:c.281A>C NP_003311.2:p.Lys94Thr
NM_177972.2:c.116A>C NP_813977.1:p.Lys39Thr
XM_005253109.2:c.242A>C XP_005253166.1:p.Lys81Thr
XM_011520344.1:c.152A>C XP_011518646.1:p.Lys51Thr
XM_005253109.3:c.242A>C XP_005253166.1:p.Lys81Thr
XM_011520344.2:c.152A>C XP_011518646.1:p.Lys51Thr
NM_177972.3:c.116A>C MANE Select NP_813977.1:p.Lys39Thr
NM_003320.5:c.281A>C NP_003311.2:p.Lys94Thr