Canonical Allele Identifier: CA379562618

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111638A>C (hg19) ; chr11:g.8090091A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090091A>C , CM000673.2:g.8090091A>C	GRCh38
NC_000011.9:g.8111638A>C , CM000673.1:g.8111638A>C	GRCh37
NC_000011.8:g.8068214A>C	NCBI36
NG_029912.1:g.56459A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.113A>C MANE Select	ENSP00000299506.3:p.Gln38Pro
ENST00000299506.2:c.113A>C	ENSP00000299506.2:p.Gln38Pro
ENST00000305253.8:c.278A>C	ENSP00000305426.4:p.Gln93Pro
ENST00000534099.5:c.131A>C	ENSP00000434400.1:p.Gln44Pro
NM_003320.4:c.278A>C	NP_003311.2:p.Gln93Pro
NM_177972.2:c.113A>C	NP_813977.1:p.Gln38Pro
XM_005253109.2:c.239A>C	XP_005253166.1:p.Gln80Pro
XM_011520344.1:c.149A>C	XP_011518646.1:p.Gln50Pro
XM_005253109.3:c.239A>C	XP_005253166.1:p.Gln80Pro
XM_011520344.2:c.149A>C	XP_011518646.1:p.Gln50Pro
NM_177972.3:c.113A>C MANE Select	NP_813977.1:p.Gln38Pro
NM_003320.5:c.278A>C	NP_003311.2:p.Gln93Pro