Canonical Allele Identifier: CA379562795

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111679G>C (hg19) ; chr11:g.8090132G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090132G>C , CM000673.2:g.8090132G>C	GRCh38
NC_000011.9:g.8111679G>C , CM000673.1:g.8111679G>C	GRCh37
NC_000011.8:g.8068255G>C	NCBI36
NG_029912.1:g.56500G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.154G>C MANE Select	ENSP00000299506.3:p.Ala52Pro
ENST00000299506.2:c.154G>C	ENSP00000299506.2:p.Ala52Pro
ENST00000305253.8:c.319G>C	ENSP00000305426.4:p.Ala107Pro
ENST00000534099.5:c.172G>C	ENSP00000434400.1:p.Ala58Pro
NM_003320.4:c.319G>C	NP_003311.2:p.Ala107Pro
NM_177972.2:c.154G>C	NP_813977.1:p.Ala52Pro
XM_005253109.2:c.280G>C	XP_005253166.1:p.Ala94Pro
XM_011520344.1:c.190G>C	XP_011518646.1:p.Ala64Pro
XM_005253109.3:c.280G>C	XP_005253166.1:p.Ala94Pro
XM_011520344.2:c.190G>C	XP_011518646.1:p.Ala64Pro
NM_177972.3:c.154G>C MANE Select	NP_813977.1:p.Ala52Pro
NM_003320.5:c.319G>C	NP_003311.2:p.Ala107Pro