Canonical Allele Identifier: CA379562626
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090093A>C , CM000673.2:g.8090093A>C GRCh38
NC_000011.9:g.8111640A>C , CM000673.1:g.8111640A>C GRCh37
NC_000011.8:g.8068216A>C NCBI36
NG_029912.1:g.56461A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.115A>C MANE Select ENSP00000299506.3:p.Lys39Gln
ENST00000299506.2:c.115A>C ENSP00000299506.2:p.Lys39Gln
ENST00000305253.8:c.280A>C ENSP00000305426.4:p.Lys94Gln
ENST00000534099.5:c.133A>C ENSP00000434400.1:p.Lys45Gln
NM_003320.4:c.280A>C NP_003311.2:p.Lys94Gln
NM_177972.2:c.115A>C NP_813977.1:p.Lys39Gln
XM_005253109.2:c.241A>C XP_005253166.1:p.Lys81Gln
XM_011520344.1:c.151A>C XP_011518646.1:p.Lys51Gln
XM_005253109.3:c.241A>C XP_005253166.1:p.Lys81Gln
XM_011520344.2:c.151A>C XP_011518646.1:p.Lys51Gln
NM_177972.3:c.115A>C MANE Select NP_813977.1:p.Lys39Gln
NM_003320.5:c.280A>C NP_003311.2:p.Lys94Gln