Canonical Allele Identifier: CA412103373
Gene: TUBGCP6 HGNC NCBI

Linked Data

dbSNP Id: rs2064576564

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50224511C>T , CM000684.2:g.50224511C>T GRCh38
NC_000022.10:g.50662940C>T , CM000684.1:g.50662940C>T GRCh37
NC_000022.9:g.49005067C>T NCBI36
NG_032160.1:g.25461G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000248846.10:c.2065G>A MANE Select ENSP00000248846.5:p.Asp689Asn
ENST00000248846.9:c.2065G>A ENSP00000248846.5:p.Asp689Asn
ENST00000439308.6:c.2065G>A ENSP00000397387.2:p.Asp689Asn
ENST00000473946.1:n.374G>A
ENST00000489511.5:n.82G>A
ENST00000491449.5:n.372G>A
ENST00000498611.5:n.2598G>A
NM_020461.3:c.2065G>A NP_065194.2:p.Asp689Asn
XR_938347.1:n.2630G>A
XR_938348.1:n.2630G>A
XR_001755343.2:n.2634G>A
XR_001755344.2:n.2634G>A
XR_002958720.1:n.2634G>A
XR_938347.2:n.2634G>A
NM_020461.4:c.2065G>A MANE Select NP_065194.3:p.Asp689Asn