Canonical Allele Identifier: CA680747486

Gene: TUB

Linked Data

• dbSNP Id: rs1270392474
• MyVariant Identifiers: chr11:g.8111707del (hg19) ; chr11:g.8090160del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000011.10:g.8090162del , CM000673.2:g.8090162del	GRCh38
NC_000011.9:g.8111709del , CM000673.1:g.8111709del	GRCh37
NC_000011.8:g.8068285del	NCBI36
NG_029912.1:g.56530del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000299506.3:c.184del MANE Select	ENSP00000299506.3:p.Arg62GlyfsTer?
ENST00000299506.2:c.184del	ENSP00000299506.2:p.Arg62GlyfsTer?
ENST00000305253.8:c.349del	ENSP00000305426.4:p.Arg117GlyfsTer?
ENST00000534099.5:c.202del	ENSP00000434400.1:p.Arg68GlyfsTer?
NM_003320.4:c.349del	NP_003311.2:p.Arg117GlyfsTer?
NM_177972.2:c.184del	NP_813977.1:p.Arg62GlyfsTer?
XM_005253109.2:c.310del	XP_005253166.1:p.Arg104GlyfsTer?
XM_011520344.1:c.220del	XP_011518646.1:p.Arg74GlyfsTer?
XM_005253109.3:c.310del	XP_005253166.1:p.Arg104GlyfsTer?
XM_011520344.2:c.220del	XP_011518646.1:p.Arg74GlyfsTer?
NM_177972.3:c.184del MANE Select	NP_813977.1:p.Arg62GlyfsTer?
NM_003320.5:c.349del	NP_003311.2:p.Arg117GlyfsTer?