Canonical Allele Identifier: CA412178190
Gene: TUBGCP6 HGNC NCBI

Linked Data

dbSNP Id: rs1273540838

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50220502G>A , CM000684.2:g.50220502G>A GRCh38
NC_000022.10:g.50658931G>A , CM000684.1:g.50658931G>A GRCh37
NC_000022.9:g.49001058G>A NCBI36
NG_032160.1:g.29470C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3857C>T MANE Select ENSP00000248846.5:p.Ala1286Val
ENST00000248846.9:c.3857C>T ENSP00000248846.5:p.Ala1286Val
ENST00000439308.6:c.3857C>T ENSP00000397387.2:p.Ala1286Val
ENST00000491449.5:n.2164C>T
ENST00000498611.5:n.3618-487C>T
NM_020461.3:c.3857C>T NP_065194.2:p.Ala1286Val
XR_938347.1:n.4422C>T
XR_938348.1:n.3050-487C>T
XR_001755343.2:n.4426C>T
XR_001755344.2:n.4426C>T
XR_002958720.1:n.3054-487C>T
XR_938347.2:n.4426C>T
NM_020461.4:c.3857C>T MANE Select NP_065194.3:p.Ala1286Val