Canonical Allele Identifier: CA473009024

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111205G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089658G>C , CM000673.2:g.8089658G>C	GRCh38
NC_000011.9:g.8111205G>C , CM000673.1:g.8111205G>C	GRCh37
NC_000011.8:g.8067781G>C	NCBI36
NG_029912.1:g.56026G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.87G>C MANE Select	ENSP00000299506.3:p.Arg29=
ENST00000299506.2:c.87G>C	ENSP00000299506.2:p.Arg29=
ENST00000305253.8:c.252G>C	ENSP00000305426.4:p.Arg84=
ENST00000534099.5:c.105G>C	ENSP00000434400.1:p.Arg35=
NM_003320.4:c.252G>C	NP_003311.2:p.Arg84=
NM_177972.2:c.87G>C	NP_813977.1:p.Arg29=
XM_005253109.2:c.213G>C	XP_005253166.1:p.Arg71=
XM_011520344.1:c.123G>C	XP_011518646.1:p.Arg41=
XM_005253109.3:c.213G>C	XP_005253166.1:p.Arg71=
XM_011520344.2:c.123G>C	XP_011518646.1:p.Arg41=
NM_177972.3:c.87G>C MANE Select	NP_813977.1:p.Arg29=
NM_003320.5:c.252G>C	NP_003311.2:p.Arg84=