Canonical Allele Identifier: CA412185152
Gene: TUBGCP6 HGNC NCBI

Linked Data

dbSNP Id: rs1555907559

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50221301G>A , CM000684.2:g.50221301G>A GRCh38
NC_000022.10:g.50659730G>A , CM000684.1:g.50659730G>A GRCh37
NC_000022.9:g.49001857G>A NCBI36
NG_032160.1:g.28671C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3058C>T MANE Select ENSP00000248846.5:p.Gln1020Ter
ENST00000248846.9:c.3058C>T ENSP00000248846.5:p.Gln1020Ter
ENST00000439308.6:c.3058C>T ENSP00000397387.2:p.Gln1020Ter
ENST00000491449.5:n.1365C>T
ENST00000498611.5:n.3591C>T
NM_020461.3:c.3058C>T NP_065194.2:p.Gln1020Ter
XR_938347.1:n.3623C>T
XR_938348.1:n.3049+727C>T
XR_001755343.2:n.3627C>T
XR_001755344.2:n.3627C>T
XR_002958720.1:n.3053+727C>T
XR_938347.2:n.3627C>T
NM_020461.4:c.3058C>T MANE Select NP_065194.3:p.Gln1020Ter