Canonical Allele Identifier: CA379562560
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090076T>G , CM000673.2:g.8090076T>G GRCh38
NC_000011.9:g.8111623T>G , CM000673.1:g.8111623T>G GRCh37
NC_000011.8:g.8068199T>G NCBI36
NG_029912.1:g.56444T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.98T>G MANE Select ENSP00000299506.3:p.Leu33Arg
ENST00000299506.2:c.98T>G ENSP00000299506.2:p.Leu33Arg
ENST00000305253.8:c.263T>G ENSP00000305426.4:p.Leu88Arg
ENST00000534099.5:c.116T>G ENSP00000434400.1:p.Leu39Arg
NM_003320.4:c.263T>G NP_003311.2:p.Leu88Arg
NM_177972.2:c.98T>G NP_813977.1:p.Leu33Arg
XM_005253109.2:c.224T>G XP_005253166.1:p.Leu75Arg
XM_011520344.1:c.134T>G XP_011518646.1:p.Leu45Arg
XM_005253109.3:c.224T>G XP_005253166.1:p.Leu75Arg
XM_011520344.2:c.134T>G XP_011518646.1:p.Leu45Arg
NM_177972.3:c.98T>G MANE Select NP_813977.1:p.Leu33Arg
NM_003320.5:c.263T>G NP_003311.2:p.Leu88Arg