Canonical Allele Identifier: CA412182519
Gene: TUBGCP6 HGNC NCBI

Linked Data

dbSNP Id: rs1205102903

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50220928A>G , CM000684.2:g.50220928A>G GRCh38
NC_000022.10:g.50659357A>G , CM000684.1:g.50659357A>G GRCh37
NC_000022.9:g.49001484A>G NCBI36
NG_032160.1:g.29044T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3431T>C MANE Select ENSP00000248846.5:p.Val1144Ala
ENST00000248846.9:c.3431T>C ENSP00000248846.5:p.Val1144Ala
ENST00000439308.6:c.3431T>C ENSP00000397387.2:p.Val1144Ala
ENST00000491449.5:n.1738T>C
ENST00000498611.5:n.3617+347T>C
NM_020461.3:c.3431T>C NP_065194.2:p.Val1144Ala
XR_938347.1:n.3996T>C
XR_938348.1:n.3050-913T>C
XR_001755343.2:n.4000T>C
XR_001755344.2:n.4000T>C
XR_002958720.1:n.3054-913T>C
XR_938347.2:n.4000T>C
NM_020461.4:c.3431T>C MANE Select NP_065194.3:p.Val1144Ala