Canonical Allele Identifier: CA2410730405
Gene: TUBGCP6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50220633_50220714delinsATGGGTGTTGCACCGTGACCGGATGGGAGCCACGTCCGATACGTTCTCCCCAACCCTGATGCTGGTGTCAGACACATGTCCG , CM000684.2:g.50220633_50220714delinsATGGGTGTTGCACCGTGACCGGATGGGAGCCACGTCCGATACGTTCTCCCCAACCCTGATGCTGGTGTCAGACACATGTCCG GRCh38
NC_000022.10:g.50659062_50659143delinsATGGGTGTTGCACCGTGACCGGATGGGAGCCACGTCCGATACGTTCTCCCCAACCCTGATGCTGGTGTCAGACACATGTCCG , CM000684.1:g.50659062_50659143delinsATGGGTGTTGCACCGTGACCGGATGGGAGCCACGTCCGATACGTTCTCCCCAACCCTGATGCTGGTGTCAGACACATGTCCG GRCh37
NC_000022.9:g.49001189_49001270delinsATGGGTGTTGCACCGTGACCGGATGGGAGCCACGTCCGATACGTTCTCCCCAACCCTGATGCTGGTGTCAGACACATGTCCG NCBI36
NG_032160.1:g.29258_29339delinsCGGACATGTGTCTGACACCAGCATCAGGGTTGGGGAGAACGTATCGGACGTGGCTCCCATCCGGTCACGGTGCAACACCCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3645_3726delinsCGGACATGTGTCTGACACCAGCATCAGGGTTGGGGAGAACGTATCGGACGTGGCTCCCATCCGGTCACGGTGCAACACCCAT MANE Select ENSP00000248846.5:p.His1215=
ENST00000248846.9:c.3645_3726delinsCGGACATGTGTCTGACACCAGCATCAGGGTTGGGGAGAACGTATCGGACGTGGCTCCCATCCGGTCACGGTGCAACACCCAT ENSP00000248846.5:p.His1215=
ENST00000439308.6:c.3645_3726delinsCGGACATGTGTCTGACACCAGCATCAGGGTTGGGGAGAACGTATCGGACGTGGCTCCCATCCGGTCACGGTGCAACACCCAT ENSP00000397387.2:p.His1215=
ENST00000491449.5:n.1952_2033delinsCGGACATGTGTCTGACACCAGCATCAGGGTTGGGGAGAACGTATCGGACGTGGCTCCCATCCGGTCACGGTGCAACACCCAT
ENST00000498611.5:n.3617+561_3618-618delinsCGGACATGTGTCTGACACCAGCATCAGGGTTGGGGAGAACGTATCGGACGTGGCTCCCATCCGGTCACGGTGCAACACCCAT
NM_020461.3:c.3645_3726delinsCGGACATGTGTCTGACACCAGCATCAGGGTTGGGGAGAACGTATCGGACGTGGCTCCCATCCGGTCACGGTGCAACACCCAT NP_065194.2:p.His1215=
XR_938347.1:n.4210_4291delinsCGGACATGTGTCTGACACCAGCATCAGGGTTGGGGAGAACGTATCGGACGTGGCTCCCATCCGGTCACGGTGCAACACCCAT
XR_938348.1:n.3050-699_3050-618delinsCGGACATGTGTCTGACACCAGCATCAGGGTTGGGGAGAACGTATCGGACGTGGCTCCCATCCGGTCACGGTGCAACACCCAT
XR_001755343.2:n.4214_4295delinsCGGACATGTGTCTGACACCAGCATCAGGGTTGGGGAGAACGTATCGGACGTGGCTCCCATCCGGTCACGGTGCAACACCCAT
XR_001755344.2:n.4214_4295delinsCGGACATGTGTCTGACACCAGCATCAGGGTTGGGGAGAACGTATCGGACGTGGCTCCCATCCGGTCACGGTGCAACACCCAT
XR_002958720.1:n.3054-699_3054-618delinsCGGACATGTGTCTGACACCAGCATCAGGGTTGGGGAGAACGTATCGGACGTGGCTCCCATCCGGTCACGGTGCAACACCCAT
XR_938347.2:n.4214_4295delinsCGGACATGTGTCTGACACCAGCATCAGGGTTGGGGAGAACGTATCGGACGTGGCTCCCATCCGGTCACGGTGCAACACCCAT
NM_020461.4:c.3645_3726delinsCGGACATGTGTCTGACACCAGCATCAGGGTTGGGGAGAACGTATCGGACGTGGCTCCCATCCGGTCACGGTGCAACACCCAT MANE Select NP_065194.3:p.His1215=