Canonical Allele Identifier: CA2410730573
Gene: TUBGCP6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50220876_50220957delinsATGGGTGTTCCACCGTGGCCGGGTGGGAGCCACGTCCGACACGTTCTCCCCAACCCTGATGCTGGCGTTGGACACGTGCCCG , CM000684.2:g.50220876_50220957delinsATGGGTGTTCCACCGTGGCCGGGTGGGAGCCACGTCCGACACGTTCTCCCCAACCCTGATGCTGGCGTTGGACACGTGCCCG GRCh38
NC_000022.10:g.50659305_50659386delinsATGGGTGTTCCACCGTGGCCGGGTGGGAGCCACGTCCGACACGTTCTCCCCAACCCTGATGCTGGCGTTGGACACGTGCCCG , CM000684.1:g.50659305_50659386delinsATGGGTGTTCCACCGTGGCCGGGTGGGAGCCACGTCCGACACGTTCTCCCCAACCCTGATGCTGGCGTTGGACACGTGCCCG GRCh37
NC_000022.9:g.49001432_49001513delinsATGGGTGTTCCACCGTGGCCGGGTGGGAGCCACGTCCGACACGTTCTCCCCAACCCTGATGCTGGCGTTGGACACGTGCCCG NCBI36
NG_032160.1:g.29015_29096delinsCGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCCGGCCACGGTGGAACACCCAT

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3402_3483delinsCGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCCGGCCACGGTGGAACACCCAT MANE Select ENSP00000248846.5:p.His1134=
ENST00000248846.9:c.3402_3483delinsCGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCCGGCCACGGTGGAACACCCAT ENSP00000248846.5:p.His1134=
ENST00000439308.6:c.3402_3483delinsCGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCCGGCCACGGTGGAACACCCAT ENSP00000397387.2:p.His1134=
ENST00000491449.5:n.1709_1790delinsCGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCCGGCCACGGTGGAACACCCAT
ENST00000498611.5:n.3617+318_3617+399delinsCGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCCGGCCACGGTGGAACACCCAT
NM_020461.3:c.3402_3483delinsCGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCCGGCCACGGTGGAACACCCAT NP_065194.2:p.His1134=
XR_938347.1:n.3967_4048delinsCGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCCGGCCACGGTGGAACACCCAT
XR_938348.1:n.3050-942_3050-861delinsCGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCCGGCCACGGTGGAACACCCAT
XR_001755343.2:n.3971_4052delinsCGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCCGGCCACGGTGGAACACCCAT
XR_001755344.2:n.3971_4052delinsCGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCCGGCCACGGTGGAACACCCAT
XR_002958720.1:n.3054-942_3054-861delinsCGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCCGGCCACGGTGGAACACCCAT
XR_938347.2:n.3971_4052delinsCGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCCGGCCACGGTGGAACACCCAT
NM_020461.4:c.3402_3483delinsCGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCCGGCCACGGTGGAACACCCAT MANE Select NP_065194.3:p.His1134=