Canonical Allele Identifier: CA379562416

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111198T>C (hg19) ; chr11:g.8089651T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089651T>C , CM000673.2:g.8089651T>C	GRCh38
NC_000011.9:g.8111198T>C , CM000673.1:g.8111198T>C	GRCh37
NC_000011.8:g.8067774T>C	NCBI36
NG_029912.1:g.56019T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.80T>C MANE Select	ENSP00000299506.3:p.Leu27Pro
ENST00000299506.2:c.80T>C	ENSP00000299506.2:p.Leu27Pro
ENST00000305253.8:c.245T>C	ENSP00000305426.4:p.Leu82Pro
ENST00000534099.5:c.98T>C	ENSP00000434400.1:p.Leu33Pro
NM_003320.4:c.245T>C	NP_003311.2:p.Leu82Pro
NM_177972.2:c.80T>C	NP_813977.1:p.Leu27Pro
XM_005253109.2:c.206T>C	XP_005253166.1:p.Leu69Pro
XM_011520344.1:c.116T>C	XP_011518646.1:p.Leu39Pro
XM_005253109.3:c.206T>C	XP_005253166.1:p.Leu69Pro
XM_011520344.2:c.116T>C	XP_011518646.1:p.Leu39Pro
NM_177972.3:c.80T>C MANE Select	NP_813977.1:p.Leu27Pro
NM_003320.5:c.245T>C	NP_003311.2:p.Leu82Pro