Canonical Allele Identifier: CA379562587
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090083G>C , CM000673.2:g.8090083G>C GRCh38
NC_000011.9:g.8111630G>C , CM000673.1:g.8111630G>C GRCh37
NC_000011.8:g.8068206G>C NCBI36
NG_029912.1:g.56451G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.105G>C MANE Select ENSP00000299506.3:p.Glu35Asp
ENST00000299506.2:c.105G>C ENSP00000299506.2:p.Glu35Asp
ENST00000305253.8:c.270G>C ENSP00000305426.4:p.Glu90Asp
ENST00000534099.5:c.123G>C ENSP00000434400.1:p.Glu41Asp
NM_003320.4:c.270G>C NP_003311.2:p.Glu90Asp
NM_177972.2:c.105G>C NP_813977.1:p.Glu35Asp
XM_005253109.2:c.231G>C XP_005253166.1:p.Glu77Asp
XM_011520344.1:c.141G>C XP_011518646.1:p.Glu47Asp
XM_005253109.3:c.231G>C XP_005253166.1:p.Glu77Asp
XM_011520344.2:c.141G>C XP_011518646.1:p.Glu47Asp
NM_177972.3:c.105G>C MANE Select NP_813977.1:p.Glu35Asp
NM_003320.5:c.270G>C NP_003311.2:p.Glu90Asp