Canonical Allele Identifier: CA412103015
Gene: TUBGCP6 HGNC NCBI

Linked Data

dbSNP Id: rs780375774

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50224372T>G , CM000684.2:g.50224372T>G GRCh38
NC_000022.10:g.50662801T>G , CM000684.1:g.50662801T>G GRCh37
NC_000022.9:g.49004928T>G NCBI36
NG_032160.1:g.25600A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.2114A>C MANE Select ENSP00000248846.5:p.Gln705Pro
ENST00000248846.9:c.2114A>C ENSP00000248846.5:p.Gln705Pro
ENST00000439308.6:c.2114A>C ENSP00000397387.2:p.Gln705Pro
ENST00000473946.1:n.423A>C
ENST00000489511.5:n.131A>C
ENST00000491449.5:n.421A>C
ENST00000498611.5:n.2647A>C
NM_020461.3:c.2114A>C NP_065194.2:p.Gln705Pro
XR_938347.1:n.2679A>C
XR_938348.1:n.2679A>C
XR_001755343.2:n.2683A>C
XR_001755344.2:n.2683A>C
XR_002958720.1:n.2683A>C
XR_938347.2:n.2683A>C
NM_020461.4:c.2114A>C MANE Select NP_065194.3:p.Gln705Pro