Canonical Allele Identifier: CA473009061

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111669G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090122G>C , CM000673.2:g.8090122G>C	GRCh38
NC_000011.9:g.8111669G>C , CM000673.1:g.8111669G>C	GRCh37
NC_000011.8:g.8068245G>C	NCBI36
NG_029912.1:g.56490G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.144G>C MANE Select	ENSP00000299506.3:p.Val48=
ENST00000299506.2:c.144G>C	ENSP00000299506.2:p.Val48=
ENST00000305253.8:c.309G>C	ENSP00000305426.4:p.Val103=
ENST00000534099.5:c.162G>C	ENSP00000434400.1:p.Val54=
NM_003320.4:c.309G>C	NP_003311.2:p.Val103=
NM_177972.2:c.144G>C	NP_813977.1:p.Val48=
XM_005253109.2:c.270G>C	XP_005253166.1:p.Val90=
XM_011520344.1:c.180G>C	XP_011518646.1:p.Val60=
XM_005253109.3:c.270G>C	XP_005253166.1:p.Val90=
XM_011520344.2:c.180G>C	XP_011518646.1:p.Val60=
NM_177972.3:c.144G>C MANE Select	NP_813977.1:p.Val48=
NM_003320.5:c.309G>C	NP_003311.2:p.Val103=