Canonical Allele Identifier: CA473009054

Gene: TUB

Linked Data

• gnomAD v4: 11-8090113-C-G
• MyVariant Identifiers: chr11:g.8111660C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090113C>G , CM000673.2:g.8090113C>G	GRCh38
NC_000011.9:g.8111660C>G , CM000673.1:g.8111660C>G	GRCh37
NC_000011.8:g.8068236C>G	NCBI36
NG_029912.1:g.56481C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.135C>G MANE Select	ENSP00000299506.3:p.Pro45=
ENST00000299506.2:c.135C>G	ENSP00000299506.2:p.Pro45=
ENST00000305253.8:c.300C>G	ENSP00000305426.4:p.Pro100=
ENST00000534099.5:c.153C>G	ENSP00000434400.1:p.Pro51=
NM_003320.4:c.300C>G	NP_003311.2:p.Pro100=
NM_177972.2:c.135C>G	NP_813977.1:p.Pro45=
XM_005253109.2:c.261C>G	XP_005253166.1:p.Pro87=
XM_011520344.1:c.171C>G	XP_011518646.1:p.Pro57=
XM_005253109.3:c.261C>G	XP_005253166.1:p.Pro87=
XM_011520344.2:c.171C>G	XP_011518646.1:p.Pro57=
NM_177972.3:c.135C>G MANE Select	NP_813977.1:p.Pro45=
NM_003320.5:c.300C>G	NP_003311.2:p.Pro100=