Canonical Allele Identifier: CA473009001

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111160C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089613C>G , CM000673.2:g.8089613C>G	GRCh38
NC_000011.9:g.8111160C>G , CM000673.1:g.8111160C>G	GRCh37
NC_000011.8:g.8067736C>G	NCBI36
NG_029912.1:g.55981C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.42C>G MANE Select	ENSP00000299506.3:p.Val14=
ENST00000299506.2:c.42C>G	ENSP00000299506.2:p.Val14=
ENST00000305253.8:c.207C>G	ENSP00000305426.4:p.Val69=
ENST00000534099.5:c.60C>G	ENSP00000434400.1:p.Val20=
NM_003320.4:c.207C>G	NP_003311.2:p.Val69=
NM_177972.2:c.42C>G	NP_813977.1:p.Val14=
XM_005253109.2:c.168C>G	XP_005253166.1:p.Val56=
XM_011520344.1:c.78C>G	XP_011518646.1:p.Val26=
XM_005253109.3:c.168C>G	XP_005253166.1:p.Val56=
XM_011520344.2:c.78C>G	XP_011518646.1:p.Val26=
NM_177972.3:c.42C>G MANE Select	NP_813977.1:p.Val14=
NM_003320.5:c.207C>G	NP_003311.2:p.Val69=