Canonical Allele Identifier: CA379562335

Gene: TUB

Linked Data

• MyVariant Identifiers: chr11:g.8111179A>C (hg19) ; chr11:g.8089632A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8089632A>C , CM000673.2:g.8089632A>C	GRCh38
NC_000011.9:g.8111179A>C , CM000673.1:g.8111179A>C	GRCh37
NC_000011.8:g.8067755A>C	NCBI36
NG_029912.1:g.56000A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.61A>C MANE Select	ENSP00000299506.3:p.Asn21His
ENST00000299506.2:c.61A>C	ENSP00000299506.2:p.Asn21His
ENST00000305253.8:c.226A>C	ENSP00000305426.4:p.Asn76His
ENST00000534099.5:c.79A>C	ENSP00000434400.1:p.Asn27His
NM_003320.4:c.226A>C	NP_003311.2:p.Asn76His
NM_177972.2:c.61A>C	NP_813977.1:p.Asn21His
XM_005253109.2:c.187A>C	XP_005253166.1:p.Asn63His
XM_011520344.1:c.97A>C	XP_011518646.1:p.Asn33His
XM_005253109.3:c.187A>C	XP_005253166.1:p.Asn63His
XM_011520344.2:c.97A>C	XP_011518646.1:p.Asn33His
NM_177972.3:c.61A>C MANE Select	NP_813977.1:p.Asn21His
NM_003320.5:c.226A>C	NP_003311.2:p.Asn76His