Canonical Allele Identifier: CA379562659
Gene: TUB HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090099A>G , CM000673.2:g.8090099A>G GRCh38
NC_000011.9:g.8111646A>G , CM000673.1:g.8111646A>G GRCh37
NC_000011.8:g.8068222A>G NCBI36
NG_029912.1:g.56467A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.121A>G MANE Select ENSP00000299506.3:p.Lys41Glu
ENST00000299506.2:c.121A>G ENSP00000299506.2:p.Lys41Glu
ENST00000305253.8:c.286A>G ENSP00000305426.4:p.Lys96Glu
ENST00000534099.5:c.139A>G ENSP00000434400.1:p.Lys47Glu
NM_003320.4:c.286A>G NP_003311.2:p.Lys96Glu
NM_177972.2:c.121A>G NP_813977.1:p.Lys41Glu
XM_005253109.2:c.247A>G XP_005253166.1:p.Lys83Glu
XM_011520344.1:c.157A>G XP_011518646.1:p.Lys53Glu
XM_005253109.3:c.247A>G XP_005253166.1:p.Lys83Glu
XM_011520344.2:c.157A>G XP_011518646.1:p.Lys53Glu
NM_177972.3:c.121A>G MANE Select NP_813977.1:p.Lys41Glu
NM_003320.5:c.286A>G NP_003311.2:p.Lys96Glu