Canonical Allele Identifier: CA379562255
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089615T>G , CM000673.2:g.8089615T>G GRCh38
NC_000011.9:g.8111162T>G , CM000673.1:g.8111162T>G GRCh37
NC_000011.8:g.8067738T>G NCBI36
NG_029912.1:g.55983T>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.44T>G MANE Select ENSP00000299506.3:p.Leu15Ter
ENST00000299506.2:c.44T>G ENSP00000299506.2:p.Leu15Ter
ENST00000305253.8:c.209T>G ENSP00000305426.4:p.Leu70Ter
ENST00000534099.5:c.62T>G ENSP00000434400.1:p.Leu21Ter
NM_003320.4:c.209T>G NP_003311.2:p.Leu70Ter
NM_177972.2:c.44T>G NP_813977.1:p.Leu15Ter
XM_005253109.2:c.170T>G XP_005253166.1:p.Leu57Ter
XM_011520344.1:c.80T>G XP_011518646.1:p.Leu27Ter
XM_005253109.3:c.170T>G XP_005253166.1:p.Leu57Ter
XM_011520344.2:c.80T>G XP_011518646.1:p.Leu27Ter
NM_177972.3:c.44T>G MANE Select NP_813977.1:p.Leu15Ter
NM_003320.5:c.209T>G NP_003311.2:p.Leu70Ter