Canonical Allele Identifier: CA379562411
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089650C>A , CM000673.2:g.8089650C>A GRCh38
NC_000011.9:g.8111197C>A , CM000673.1:g.8111197C>A GRCh37
NC_000011.8:g.8067773C>A NCBI36
NG_029912.1:g.56018C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.79C>A MANE Select ENSP00000299506.3:p.Leu27Ile
ENST00000299506.2:c.79C>A ENSP00000299506.2:p.Leu27Ile
ENST00000305253.8:c.244C>A ENSP00000305426.4:p.Leu82Ile
ENST00000534099.5:c.97C>A ENSP00000434400.1:p.Leu33Ile
NM_003320.4:c.244C>A NP_003311.2:p.Leu82Ile
NM_177972.2:c.79C>A NP_813977.1:p.Leu27Ile
XM_005253109.2:c.205C>A XP_005253166.1:p.Leu69Ile
XM_011520344.1:c.115C>A XP_011518646.1:p.Leu39Ile
XM_005253109.3:c.205C>A XP_005253166.1:p.Leu69Ile
XM_011520344.2:c.115C>A XP_011518646.1:p.Leu39Ile
NM_177972.3:c.79C>A MANE Select NP_813977.1:p.Leu27Ile
NM_003320.5:c.244C>A NP_003311.2:p.Leu82Ile