Canonical Allele Identifier: CA379563131
Gene: TUB HGNC NCBI

Linked Data

dbSNP Id: rs1943746124

Genomic Alleles

HGVS Genome Assembly
NC_000011.10:g.8090211G>A , CM000673.2:g.8090211G>A GRCh38
NC_000011.9:g.8111758G>A , CM000673.1:g.8111758G>A GRCh37
NC_000011.8:g.8068334G>A NCBI36
NG_029912.1:g.56579G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000299506.3:c.233G>A MANE Select ENSP00000299506.3:p.Ser78Asn
ENST00000299506.2:c.233G>A ENSP00000299506.2:p.Ser78Asn
ENST00000305253.8:c.398G>A ENSP00000305426.4:p.Ser133Asn
ENST00000534099.5:c.251G>A ENSP00000434400.1:p.Ser84Asn
NM_003320.4:c.398G>A NP_003311.2:p.Ser133Asn
NM_177972.2:c.233G>A NP_813977.1:p.Ser78Asn
XM_005253109.2:c.359G>A XP_005253166.1:p.Ser120Asn
XM_011520344.1:c.269G>A XP_011518646.1:p.Ser90Asn
XM_005253109.3:c.359G>A XP_005253166.1:p.Ser120Asn
XM_011520344.2:c.269G>A XP_011518646.1:p.Ser90Asn
NM_177972.3:c.233G>A MANE Select NP_813977.1:p.Ser78Asn
NM_003320.5:c.398G>A NP_003311.2:p.Ser133Asn