Canonical Allele Identifier: CA412177886
Gene: TUBGCP6 HGNC NCBI

Linked Data

dbSNP Id: rs142063347

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50220467G>T , CM000684.2:g.50220467G>T GRCh38
NC_000022.10:g.50658896G>T , CM000684.1:g.50658896G>T GRCh37
NC_000022.9:g.49001023G>T NCBI36
NG_032160.1:g.29505C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3892C>A MANE Select ENSP00000248846.5:p.Pro1298Thr
ENST00000248846.9:c.3892C>A ENSP00000248846.5:p.Pro1298Thr
ENST00000439308.6:c.3892C>A ENSP00000397387.2:p.Pro1298Thr
ENST00000491449.5:n.2199C>A
ENST00000498611.5:n.3618-452C>A
NM_020461.3:c.3892C>A NP_065194.2:p.Pro1298Thr
XR_938347.1:n.4457C>A
XR_938348.1:n.3050-452C>A
XR_001755343.2:n.4461C>A
XR_001755344.2:n.4461C>A
XR_002958720.1:n.3054-452C>A
XR_938347.2:n.4461C>A
NM_020461.4:c.3892C>A MANE Select NP_065194.3:p.Pro1298Thr