Canonical Allele Identifier: CA379562773

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111673G>C (hg19) ; chr11:g.8090126G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090126G>C , CM000673.2:g.8090126G>C	GRCh38
NC_000011.9:g.8111673G>C , CM000673.1:g.8111673G>C	GRCh37
NC_000011.8:g.8068249G>C	NCBI36
NG_029912.1:g.56494G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.148G>C MANE Select	ENSP00000299506.3:p.Ala50Pro
ENST00000299506.2:c.148G>C	ENSP00000299506.2:p.Ala50Pro
ENST00000305253.8:c.313G>C	ENSP00000305426.4:p.Ala105Pro
ENST00000534099.5:c.166G>C	ENSP00000434400.1:p.Ala56Pro
NM_003320.4:c.313G>C	NP_003311.2:p.Ala105Pro
NM_177972.2:c.148G>C	NP_813977.1:p.Ala50Pro
XM_005253109.2:c.274G>C	XP_005253166.1:p.Ala92Pro
XM_011520344.1:c.184G>C	XP_011518646.1:p.Ala62Pro
XM_005253109.3:c.274G>C	XP_005253166.1:p.Ala92Pro
XM_011520344.2:c.184G>C	XP_011518646.1:p.Ala62Pro
NM_177972.3:c.148G>C MANE Select	NP_813977.1:p.Ala50Pro
NM_003320.5:c.313G>C	NP_003311.2:p.Ala105Pro