Canonical Allele Identifier: CA2410730459
Gene: TUBGCP6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50220714_50220780delinsGTGGGTGTTCCACCGTGGCCGGGTGGGAGCCATGTCTGACACAGACTCCCCCAAGCTGATGCTGGCA , CM000684.2:g.50220714_50220780delinsGTGGGTGTTCCACCGTGGCCGGGTGGGAGCCATGTCTGACACAGACTCCCCCAAGCTGATGCTGGCA GRCh38
NC_000022.10:g.50659143_50659209delinsGTGGGTGTTCCACCGTGGCCGGGTGGGAGCCATGTCTGACACAGACTCCCCCAAGCTGATGCTGGCA , CM000684.1:g.50659143_50659209delinsGTGGGTGTTCCACCGTGGCCGGGTGGGAGCCATGTCTGACACAGACTCCCCCAAGCTGATGCTGGCA GRCh37
NC_000022.9:g.49001270_49001336delinsGTGGGTGTTCCACCGTGGCCGGGTGGGAGCCATGTCTGACACAGACTCCCCCAAGCTGATGCTGGCA NCBI36
NG_032160.1:g.29192_29258delinsTGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3579_3645delinsTGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC MANE Select ENSP00000248846.5:p.Asp1193=
ENST00000248846.9:c.3579_3645delinsTGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC ENSP00000248846.5:p.Asp1193=
ENST00000439308.6:c.3579_3645delinsTGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC ENSP00000397387.2:p.Asp1193=
ENST00000491449.5:n.1886_1952delinsTGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC
ENST00000498611.5:n.3617+495_3617+561delinsTGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC
NM_020461.3:c.3579_3645delinsTGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC NP_065194.2:p.Asp1193=
XR_938347.1:n.4144_4210delinsTGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC
XR_938348.1:n.3050-765_3050-699delinsTGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC
XR_001755343.2:n.4148_4214delinsTGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC
XR_001755344.2:n.4148_4214delinsTGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC
XR_002958720.1:n.3054-765_3054-699delinsTGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC
XR_938347.2:n.4148_4214delinsTGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC
NM_020461.4:c.3579_3645delinsTGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCACCCGGCCACGGTGGAACACCCAC MANE Select NP_065194.3:p.Asp1193=