Canonical Allele Identifier: CA379562633
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.116A>T MANE Select ENSP00000299506.3:p.Lys39Met
ENST00000299506.2:c.116A>T ENSP00000299506.2:p.Lys39Met
ENST00000305253.8:c.281A>T ENSP00000305426.4:p.Lys94Met
ENST00000534099.5:c.134A>T ENSP00000434400.1:p.Lys45Met
NM_003320.4:c.281A>T NP_003311.2:p.Lys94Met
NM_177972.2:c.116A>T NP_813977.1:p.Lys39Met
XM_005253109.2:c.242A>T XP_005253166.1:p.Lys81Met
XM_011520344.1:c.152A>T XP_011518646.1:p.Lys51Met
XM_005253109.3:c.242A>T XP_005253166.1:p.Lys81Met
XM_011520344.2:c.152A>T XP_011518646.1:p.Lys51Met
NM_177972.3:c.116A>T MANE Select NP_813977.1:p.Lys39Met
NM_003320.5:c.281A>T NP_003311.2:p.Lys94Met