Canonical Allele Identifier: CA2612330581
Gene: TUB HGNC NCBI

Linked Data

gnomAD v4: 11-8090056-T-C

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090056T>C , CM000673.2:g.8090056T>C GRCh38
NC_000011.9:g.8111603T>C , CM000673.1:g.8111603T>C GRCh37
NC_000011.8:g.8068179T>C NCBI36
NG_029912.1:g.56424T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000299506.3:c.91-13T>C MANE Select ENSP00000299506.3:n.91-13T>C
ENST00000299506.2:c.91-13T>C ENSP00000299506.2:n.91-13T>C
ENST00000305253.8:c.256-13T>C ENSP00000305426.4:n.256-13T>C
ENST00000534099.5:c.109-13T>C ENSP00000434400.1:n.109-13T>C
NM_003320.4:c.256-13T>C NP_003311.2:n.256-13T>C
NM_177972.2:c.91-13T>C NP_813977.1:n.91-13T>C
XM_005253109.2:c.217-13T>C XP_005253166.1:n.217-13T>C
XM_011520344.1:c.127-13T>C XP_011518646.1:n.127-13T>C
XM_005253109.3:c.217-13T>C XP_005253166.1:n.217-13T>C
XM_011520344.2:c.127-13T>C XP_011518646.1:n.127-13T>C
NM_177972.3:c.91-13T>C MANE Select NP_813977.1:n.91-13T>C
NM_003320.5:c.256-13T>C NP_003311.2:n.256-13T>C