Canonical Allele Identifier: CA379562278
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8089621A>G , CM000673.2:g.8089621A>G GRCh38
NC_000011.9:g.8111168A>G , CM000673.1:g.8111168A>G GRCh37
NC_000011.8:g.8067744A>G NCBI36
NG_029912.1:g.55989A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.50A>G MANE Select ENSP00000299506.3:p.Asp17Gly
ENST00000299506.2:c.50A>G ENSP00000299506.2:p.Asp17Gly
ENST00000305253.8:c.215A>G ENSP00000305426.4:p.Asp72Gly
ENST00000534099.5:c.68A>G ENSP00000434400.1:p.Asp23Gly
NM_003320.4:c.215A>G NP_003311.2:p.Asp72Gly
NM_177972.2:c.50A>G NP_813977.1:p.Asp17Gly
XM_005253109.2:c.176A>G XP_005253166.1:p.Asp59Gly
XM_011520344.1:c.86A>G XP_011518646.1:p.Asp29Gly
XM_005253109.3:c.176A>G XP_005253166.1:p.Asp59Gly
XM_011520344.2:c.86A>G XP_011518646.1:p.Asp29Gly
NM_177972.3:c.50A>G MANE Select NP_813977.1:p.Asp17Gly
NM_003320.5:c.215A>G NP_003311.2:p.Asp72Gly