Canonical Allele Identifier: CA379562838
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090142G>T , CM000673.2:g.8090142G>T GRCh38
NC_000011.9:g.8111689G>T , CM000673.1:g.8111689G>T GRCh37
NC_000011.8:g.8068265G>T NCBI36
NG_029912.1:g.56510G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.164G>T MANE Select ENSP00000299506.3:p.Arg55Leu
ENST00000299506.2:c.164G>T ENSP00000299506.2:p.Arg55Leu
ENST00000305253.8:c.329G>T ENSP00000305426.4:p.Arg110Leu
ENST00000534099.5:c.182G>T ENSP00000434400.1:p.Arg61Leu
NM_003320.4:c.329G>T NP_003311.2:p.Arg110Leu
NM_177972.2:c.164G>T NP_813977.1:p.Arg55Leu
XM_005253109.2:c.290G>T XP_005253166.1:p.Arg97Leu
XM_011520344.1:c.200G>T XP_011518646.1:p.Arg67Leu
XM_005253109.3:c.290G>T XP_005253166.1:p.Arg97Leu
XM_011520344.2:c.200G>T XP_011518646.1:p.Arg67Leu
NM_177972.3:c.164G>T MANE Select NP_813977.1:p.Arg55Leu
NM_003320.5:c.329G>T NP_003311.2:p.Arg110Leu