Canonical Allele Identifier: CA2410730592

Gene: TUBGCP6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50220896_50220977delinsGGGTGGGAGCCACGTCCGACACGTTCTCCCCAACCCTGATGCTGGCGTTGGACACGTGCCCGTGGGTATTCCACCGTGGCCT , CM000684.2:g.50220896_50220977delinsGGGTGGGAGCCACGTCCGACACGTTCTCCCCAACCCTGATGCTGGCGTTGGACACGTGCCCGTGGGTATTCCACCGTGGCCT	GRCh38
NC_000022.10:g.50659325_50659406delinsGGGTGGGAGCCACGTCCGACACGTTCTCCCCAACCCTGATGCTGGCGTTGGACACGTGCCCGTGGGTATTCCACCGTGGCCT , CM000684.1:g.50659325_50659406delinsGGGTGGGAGCCACGTCCGACACGTTCTCCCCAACCCTGATGCTGGCGTTGGACACGTGCCCGTGGGTATTCCACCGTGGCCT	GRCh37
NC_000022.9:g.49001452_49001533delinsGGGTGGGAGCCACGTCCGACACGTTCTCCCCAACCCTGATGCTGGCGTTGGACACGTGCCCGTGGGTATTCCACCGTGGCCT	NCBI36
NG_032160.1:g.28995_29076delinsAGGCCACGGTGGAATACCCACGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248846.10:c.3382_3463delinsAGGCCACGGTGGAATACCCACGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCC MANE Select	ENSP00000248846.5:p.Arg1128=
ENST00000248846.9:c.3382_3463delinsAGGCCACGGTGGAATACCCACGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCC	ENSP00000248846.5:p.Arg1128=
ENST00000439308.6:c.3382_3463delinsAGGCCACGGTGGAATACCCACGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCC	ENSP00000397387.2:p.Arg1128=
ENST00000491449.5:n.1689_1770delinsAGGCCACGGTGGAATACCCACGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCC
ENST00000498611.5:n.3617+298_3617+379delinsAGGCCACGGTGGAATACCCACGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCC
NM_020461.3:c.3382_3463delinsAGGCCACGGTGGAATACCCACGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCC	NP_065194.2:p.Arg1128=
XR_938347.1:n.3947_4028delinsAGGCCACGGTGGAATACCCACGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCC
XR_938348.1:n.3050-962_3050-881delinsAGGCCACGGTGGAATACCCACGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCC
XR_001755343.2:n.3951_4032delinsAGGCCACGGTGGAATACCCACGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCC
XR_001755344.2:n.3951_4032delinsAGGCCACGGTGGAATACCCACGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCC
XR_002958720.1:n.3054-962_3054-881delinsAGGCCACGGTGGAATACCCACGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCC
XR_938347.2:n.3951_4032delinsAGGCCACGGTGGAATACCCACGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCC
NM_020461.4:c.3382_3463delinsAGGCCACGGTGGAATACCCACGGGCACGTGTCCAACGCCAGCATCAGGGTTGGGGAGAACGTGTCGGACGTGGCTCCCACCC MANE Select	NP_065194.3:p.Arg1128=