Canonical Allele Identifier: CA2410730507

Gene: TUBGCP6

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50220783_50220864delinsAGACACGTGTCCATGGGTGTTCCACCGTGGCCGGGCGGGAGCCATGTCTGACACAGACTCCCCCAAGCTGATGCTGGCATCG , CM000684.2:g.50220783_50220864delinsAGACACGTGTCCATGGGTGTTCCACCGTGGCCGGGCGGGAGCCATGTCTGACACAGACTCCCCCAAGCTGATGCTGGCATCG	GRCh38
NC_000022.10:g.50659212_50659293delinsAGACACGTGTCCATGGGTGTTCCACCGTGGCCGGGCGGGAGCCATGTCTGACACAGACTCCCCCAAGCTGATGCTGGCATCG , CM000684.1:g.50659212_50659293delinsAGACACGTGTCCATGGGTGTTCCACCGTGGCCGGGCGGGAGCCATGTCTGACACAGACTCCCCCAAGCTGATGCTGGCATCG	GRCh37
NC_000022.9:g.49001339_49001420delinsAGACACGTGTCCATGGGTGTTCCACCGTGGCCGGGCGGGAGCCATGTCTGACACAGACTCCCCCAAGCTGATGCTGGCATCG	NCBI36
NG_032160.1:g.29108_29189delinsCGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCGCCCGGCCACGGTGGAACACCCATGGACACGTGTCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248846.10:c.3495_3576delinsCGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCGCCCGGCCACGGTGGAACACCCATGGACACGTGTCT MANE Select	ENSP00000248846.5:p.Ser1165=
ENST00000248846.9:c.3495_3576delinsCGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCGCCCGGCCACGGTGGAACACCCATGGACACGTGTCT	ENSP00000248846.5:p.Ser1165=
ENST00000439308.6:c.3495_3576delinsCGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCGCCCGGCCACGGTGGAACACCCATGGACACGTGTCT	ENSP00000397387.2:p.Ser1165=
ENST00000491449.5:n.1802_1883delinsCGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCGCCCGGCCACGGTGGAACACCCATGGACACGTGTCT
ENST00000498611.5:n.3617+411_3617+492delinsCGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCGCCCGGCCACGGTGGAACACCCATGGACACGTGTCT
NM_020461.3:c.3495_3576delinsCGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCGCCCGGCCACGGTGGAACACCCATGGACACGTGTCT	NP_065194.2:p.Ser1165=
XR_938347.1:n.4060_4141delinsCGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCGCCCGGCCACGGTGGAACACCCATGGACACGTGTCT
XR_938348.1:n.3050-849_3050-768delinsCGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCGCCCGGCCACGGTGGAACACCCATGGACACGTGTCT
XR_001755343.2:n.4064_4145delinsCGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCGCCCGGCCACGGTGGAACACCCATGGACACGTGTCT
XR_001755344.2:n.4064_4145delinsCGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCGCCCGGCCACGGTGGAACACCCATGGACACGTGTCT
XR_002958720.1:n.3054-849_3054-768delinsCGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCGCCCGGCCACGGTGGAACACCCATGGACACGTGTCT
XR_938347.2:n.4064_4145delinsCGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCGCCCGGCCACGGTGGAACACCCATGGACACGTGTCT
NM_020461.4:c.3495_3576delinsCGATGCCAGCATCAGCTTGGGGGAGTCTGTGTCAGACATGGCTCCCGCCCGGCCACGGTGGAACACCCATGGACACGTGTCT MANE Select	NP_065194.3:p.Ser1165=