Canonical Allele Identifier: CA2410730477
Gene: TUBGCP6 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50220737_50220818delinsTGGGAGCCATGTCTGACACAGACTCCCCCAAGCTGATGCTGGCATCAGACACGTGTCCATGGGTGTTCCACCGTGGCCGGGC , CM000684.2:g.50220737_50220818delinsTGGGAGCCATGTCTGACACAGACTCCCCCAAGCTGATGCTGGCATCAGACACGTGTCCATGGGTGTTCCACCGTGGCCGGGC GRCh38
NC_000022.10:g.50659166_50659247delinsTGGGAGCCATGTCTGACACAGACTCCCCCAAGCTGATGCTGGCATCAGACACGTGTCCATGGGTGTTCCACCGTGGCCGGGC , CM000684.1:g.50659166_50659247delinsTGGGAGCCATGTCTGACACAGACTCCCCCAAGCTGATGCTGGCATCAGACACGTGTCCATGGGTGTTCCACCGTGGCCGGGC GRCh37
NC_000022.9:g.49001293_49001374delinsTGGGAGCCATGTCTGACACAGACTCCCCCAAGCTGATGCTGGCATCAGACACGTGTCCATGGGTGTTCCACCGTGGCCGGGC NCBI36
NG_032160.1:g.29154_29235delinsGCCCGGCCACGGTGGAACACCCATGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCA

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3541_3622delinsGCCCGGCCACGGTGGAACACCCATGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCA MANE Select ENSP00000248846.5:p.Ala1181=
ENST00000248846.9:c.3541_3622delinsGCCCGGCCACGGTGGAACACCCATGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCA ENSP00000248846.5:p.Ala1181=
ENST00000439308.6:c.3541_3622delinsGCCCGGCCACGGTGGAACACCCATGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCA ENSP00000397387.2:p.Ala1181=
ENST00000491449.5:n.1848_1929delinsGCCCGGCCACGGTGGAACACCCATGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCA
ENST00000498611.5:n.3617+457_3617+538delinsGCCCGGCCACGGTGGAACACCCATGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCA
NM_020461.3:c.3541_3622delinsGCCCGGCCACGGTGGAACACCCATGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCA NP_065194.2:p.Ala1181=
XR_938347.1:n.4106_4187delinsGCCCGGCCACGGTGGAACACCCATGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCA
XR_938348.1:n.3050-803_3050-722delinsGCCCGGCCACGGTGGAACACCCATGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCA
XR_001755343.2:n.4110_4191delinsGCCCGGCCACGGTGGAACACCCATGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCA
XR_001755344.2:n.4110_4191delinsGCCCGGCCACGGTGGAACACCCATGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCA
XR_002958720.1:n.3054-803_3054-722delinsGCCCGGCCACGGTGGAACACCCATGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCA
XR_938347.2:n.4110_4191delinsGCCCGGCCACGGTGGAACACCCATGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCA
NM_020461.4:c.3541_3622delinsGCCCGGCCACGGTGGAACACCCATGGACACGTGTCTGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCA MANE Select NP_065194.3:p.Ala1181=