Canonical Allele Identifier: CA379562733

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111665T>C (hg19) ; chr11:g.8090118T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090118T>C , CM000673.2:g.8090118T>C	GRCh38
NC_000011.9:g.8111665T>C , CM000673.1:g.8111665T>C	GRCh37
NC_000011.8:g.8068241T>C	NCBI36
NG_029912.1:g.56486T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.140T>C MANE Select	ENSP00000299506.3:p.Met47Thr
ENST00000299506.2:c.140T>C	ENSP00000299506.2:p.Met47Thr
ENST00000305253.8:c.305T>C	ENSP00000305426.4:p.Met102Thr
ENST00000534099.5:c.158T>C	ENSP00000434400.1:p.Met53Thr
NM_003320.4:c.305T>C	NP_003311.2:p.Met102Thr
NM_177972.2:c.140T>C	NP_813977.1:p.Met47Thr
XM_005253109.2:c.266T>C	XP_005253166.1:p.Met89Thr
XM_011520344.1:c.176T>C	XP_011518646.1:p.Met59Thr
XM_005253109.3:c.266T>C	XP_005253166.1:p.Met89Thr
XM_011520344.2:c.176T>C	XP_011518646.1:p.Met59Thr
NM_177972.3:c.140T>C MANE Select	NP_813977.1:p.Met47Thr
NM_003320.5:c.305T>C	NP_003311.2:p.Met102Thr