Canonical Allele Identifier: CA379562594

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111632A>C (hg19) ; chr11:g.8090085A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090085A>C , CM000673.2:g.8090085A>C	GRCh38
NC_000011.9:g.8111632A>C , CM000673.1:g.8111632A>C	GRCh37
NC_000011.8:g.8068208A>C	NCBI36
NG_029912.1:g.56453A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.107A>C MANE Select	ENSP00000299506.3:p.Gln36Pro
ENST00000299506.2:c.107A>C	ENSP00000299506.2:p.Gln36Pro
ENST00000305253.8:c.272A>C	ENSP00000305426.4:p.Gln91Pro
ENST00000534099.5:c.125A>C	ENSP00000434400.1:p.Gln42Pro
NM_003320.4:c.272A>C	NP_003311.2:p.Gln91Pro
NM_177972.2:c.107A>C	NP_813977.1:p.Gln36Pro
XM_005253109.2:c.233A>C	XP_005253166.1:p.Gln78Pro
XM_011520344.1:c.143A>C	XP_011518646.1:p.Gln48Pro
XM_005253109.3:c.233A>C	XP_005253166.1:p.Gln78Pro
XM_011520344.2:c.143A>C	XP_011518646.1:p.Gln48Pro
NM_177972.3:c.107A>C MANE Select	NP_813977.1:p.Gln36Pro
NM_003320.5:c.272A>C	NP_003311.2:p.Gln91Pro