Canonical Allele Identifier: CA2580990440
Gene: TUB HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089574C>G , CM000673.2:g.8089574C>G GRCh38
NC_000011.9:g.8111121C>G , CM000673.1:g.8111121C>G GRCh37
NC_000011.8:g.8067697C>G NCBI36
NG_029912.1:g.55942C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.39-36C>G MANE Select ENSP00000299506.3:n.39-36C>G
ENST00000299506.2:c.39-36C>G ENSP00000299506.2:n.39-36C>G
ENST00000305253.8:c.204-36C>G ENSP00000305426.4:n.204-36C>G
ENST00000534099.5:c.57-36C>G ENSP00000434400.1:n.57-36C>G
NM_003320.4:c.204-36C>G NP_003311.2:n.204-36C>G
NM_177972.2:c.39-36C>G NP_813977.1:n.39-36C>G
XM_005253109.2:c.165-36C>G XP_005253166.1:n.165-36C>G
XM_011520344.1:c.75-36C>G XP_011518646.1:n.75-36C>G
XM_005253109.3:c.165-36C>G XP_005253166.1:n.165-36C>G
XM_011520344.2:c.75-36C>G XP_011518646.1:n.75-36C>G
NM_177972.3:c.39-36C>G MANE Select NP_813977.1:n.39-36C>G
NM_003320.5:c.204-36C>G NP_003311.2:n.204-36C>G