Canonical Allele Identifier: CA2410730460
Gene: TUBGCP6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50220714_50220795delinsGTGGGTGTTCCACCGTGGCCGGGTGGGAGCCATGTCTGACACAGACTCCCCCAAGCTGATGCTGGCATCAGACACGTGTCCA , CM000684.2:g.50220714_50220795delinsGTGGGTGTTCCACCGTGGCCGGGTGGGAGCCATGTCTGACACAGACTCCCCCAAGCTGATGCTGGCATCAGACACGTGTCCA GRCh38
NC_000022.10:g.50659143_50659224delinsGTGGGTGTTCCACCGTGGCCGGGTGGGAGCCATGTCTGACACAGACTCCCCCAAGCTGATGCTGGCATCAGACACGTGTCCA , CM000684.1:g.50659143_50659224delinsGTGGGTGTTCCACCGTGGCCGGGTGGGAGCCATGTCTGACACAGACTCCCCCAAGCTGATGCTGGCATCAGACACGTGTCCA GRCh37
NC_000022.9:g.49001270_49001351delinsGTGGGTGTTCCACCGTGGCCGGGTGGGAGCCATGTCTGACACAGACTCCCCCAAGCTGATGCTGGCATCAGACACGTGTCCA NCBI36
NG_032160.1:g.29177_29258delinsTGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3564_3645delinsTGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC MANE Select ENSP00000248846.5:p.His1188=
ENST00000248846.9:c.3564_3645delinsTGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC ENSP00000248846.5:p.His1188=
ENST00000439308.6:c.3564_3645delinsTGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC ENSP00000397387.2:p.His1188=
ENST00000491449.5:n.1871_1952delinsTGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC
ENST00000498611.5:n.3617+480_3617+561delinsTGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC
NM_020461.3:c.3564_3645delinsTGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC NP_065194.2:p.His1188=
XR_938347.1:n.4129_4210delinsTGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC
XR_938348.1:n.3050-780_3050-699delinsTGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC
XR_001755343.2:n.4133_4214delinsTGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC
XR_001755344.2:n.4133_4214delinsTGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC
XR_002958720.1:n.3054-780_3054-699delinsTGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC
XR_938347.2:n.4133_4214delinsTGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC
NM_020461.4:c.3564_3645delinsTGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC MANE Select NP_065194.3:p.His1188=