Canonical Allele Identifier: CA379562298
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089625G>C , CM000673.2:g.8089625G>C GRCh38
NC_000011.9:g.8111172G>C , CM000673.1:g.8111172G>C GRCh37
NC_000011.8:g.8067748G>C NCBI36
NG_029912.1:g.55993G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.54G>C MANE Select ENSP00000299506.3:p.Glu18Asp
ENST00000299506.2:c.54G>C ENSP00000299506.2:p.Glu18Asp
ENST00000305253.8:c.219G>C ENSP00000305426.4:p.Glu73Asp
ENST00000534099.5:c.72G>C ENSP00000434400.1:p.Glu24Asp
NM_003320.4:c.219G>C NP_003311.2:p.Glu73Asp
NM_177972.2:c.54G>C NP_813977.1:p.Glu18Asp
XM_005253109.2:c.180G>C XP_005253166.1:p.Glu60Asp
XM_011520344.1:c.90G>C XP_011518646.1:p.Glu30Asp
XM_005253109.3:c.180G>C XP_005253166.1:p.Glu60Asp
XM_011520344.2:c.90G>C XP_011518646.1:p.Glu30Asp
NM_177972.3:c.54G>C MANE Select NP_813977.1:p.Glu18Asp
NM_003320.5:c.219G>C NP_003311.2:p.Glu73Asp