Canonical Allele Identifier: CA473009058

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111663G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090116G>C , CM000673.2:g.8090116G>C	GRCh38
NC_000011.9:g.8111663G>C , CM000673.1:g.8111663G>C	GRCh37
NC_000011.8:g.8068239G>C	NCBI36
NG_029912.1:g.56484G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.138G>C MANE Select	ENSP00000299506.3:p.Leu46=
ENST00000299506.2:c.138G>C	ENSP00000299506.2:p.Leu46=
ENST00000305253.8:c.303G>C	ENSP00000305426.4:p.Leu101=
ENST00000534099.5:c.156G>C	ENSP00000434400.1:p.Leu52=
NM_003320.4:c.303G>C	NP_003311.2:p.Leu101=
NM_177972.2:c.138G>C	NP_813977.1:p.Leu46=
XM_005253109.2:c.264G>C	XP_005253166.1:p.Leu88=
XM_011520344.1:c.174G>C	XP_011518646.1:p.Leu58=
XM_005253109.3:c.264G>C	XP_005253166.1:p.Leu88=
XM_011520344.2:c.174G>C	XP_011518646.1:p.Leu58=
NM_177972.3:c.138G>C MANE Select	NP_813977.1:p.Leu46=
NM_003320.5:c.303G>C	NP_003311.2:p.Leu101=