Canonical Allele Identifier: CA379562763
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090124A>G , CM000673.2:g.8090124A>G GRCh38
NC_000011.9:g.8111671A>G , CM000673.1:g.8111671A>G GRCh37
NC_000011.8:g.8068247A>G NCBI36
NG_029912.1:g.56492A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.146A>G MANE Select ENSP00000299506.3:p.Gln49Arg
ENST00000299506.2:c.146A>G ENSP00000299506.2:p.Gln49Arg
ENST00000305253.8:c.311A>G ENSP00000305426.4:p.Gln104Arg
ENST00000534099.5:c.164A>G ENSP00000434400.1:p.Gln55Arg
NM_003320.4:c.311A>G NP_003311.2:p.Gln104Arg
NM_177972.2:c.146A>G NP_813977.1:p.Gln49Arg
XM_005253109.2:c.272A>G XP_005253166.1:p.Gln91Arg
XM_011520344.1:c.182A>G XP_011518646.1:p.Gln61Arg
XM_005253109.3:c.272A>G XP_005253166.1:p.Gln91Arg
XM_011520344.2:c.182A>G XP_011518646.1:p.Gln61Arg
NM_177972.3:c.146A>G MANE Select NP_813977.1:p.Gln49Arg
NM_003320.5:c.311A>G NP_003311.2:p.Gln104Arg