Canonical Allele Identifier: CA412185022
Gene: TUBGCP6 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50221277G>T , CM000684.2:g.50221277G>T GRCh38
NC_000022.10:g.50659706G>T , CM000684.1:g.50659706G>T GRCh37
NC_000022.9:g.49001833G>T NCBI36
NG_032160.1:g.28695C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3082C>A MANE Select ENSP00000248846.5:p.Gln1028Lys
ENST00000248846.9:c.3082C>A ENSP00000248846.5:p.Gln1028Lys
ENST00000439308.6:c.3082C>A ENSP00000397387.2:p.Gln1028Lys
ENST00000491449.5:n.1389C>A
ENST00000498611.5:n.3615C>A
NM_020461.3:c.3082C>A NP_065194.2:p.Gln1028Lys
XR_938347.1:n.3647C>A
XR_938348.1:n.3049+751C>A
XR_001755343.2:n.3651C>A
XR_001755344.2:n.3651C>A
XR_002958720.1:n.3053+751C>A
XR_938347.2:n.3651C>A
NM_020461.4:c.3082C>A MANE Select NP_065194.3:p.Gln1028Lys