Canonical Allele Identifier: CA2612330446
Gene: TUB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089917G>T , CM000673.2:g.8089917G>T GRCh38
NC_000011.9:g.8111464G>T , CM000673.1:g.8111464G>T GRCh37
NC_000011.8:g.8068040G>T NCBI36
NG_029912.1:g.56285G>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.91-152G>T MANE Select ENSP00000299506.3:n.91-152G>T
ENST00000299506.2:c.91-152G>T ENSP00000299506.2:n.91-152G>T
ENST00000305253.8:c.256-152G>T ENSP00000305426.4:n.256-152G>T
ENST00000534099.5:c.109-152G>T ENSP00000434400.1:n.109-152G>T
NM_003320.4:c.256-152G>T NP_003311.2:n.256-152G>T
NM_177972.2:c.91-152G>T NP_813977.1:n.91-152G>T
XM_005253109.2:c.217-152G>T XP_005253166.1:n.217-152G>T
XM_011520344.1:c.127-152G>T XP_011518646.1:n.127-152G>T
XM_005253109.3:c.217-152G>T XP_005253166.1:n.217-152G>T
XM_011520344.2:c.127-152G>T XP_011518646.1:n.127-152G>T
NM_177972.3:c.91-152G>T MANE Select NP_813977.1:n.91-152G>T
NM_003320.5:c.256-152G>T NP_003311.2:n.256-152G>T