Canonical Allele Identifier: CA379562628
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

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

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.115A>G MANE Select ENSP00000299506.3:p.Lys39Glu
ENST00000299506.2:c.115A>G ENSP00000299506.2:p.Lys39Glu
ENST00000305253.8:c.280A>G ENSP00000305426.4:p.Lys94Glu
ENST00000534099.5:c.133A>G ENSP00000434400.1:p.Lys45Glu
NM_003320.4:c.280A>G NP_003311.2:p.Lys94Glu
NM_177972.2:c.115A>G NP_813977.1:p.Lys39Glu
XM_005253109.2:c.241A>G XP_005253166.1:p.Lys81Glu
XM_011520344.1:c.151A>G XP_011518646.1:p.Lys51Glu
XM_005253109.3:c.241A>G XP_005253166.1:p.Lys81Glu
XM_011520344.2:c.151A>G XP_011518646.1:p.Lys51Glu
NM_177972.3:c.115A>G MANE Select NP_813977.1:p.Lys39Glu
NM_003320.5:c.280A>G NP_003311.2:p.Lys94Glu