Canonical Allele Identifier: CA412103199

Gene: TUBGCP6

Linked Data

• ClinVar Variation Id: 1382361
• ClinVar RCV Id: RCV001922194
• dbSNP Id: rs2147185153
• MyVariant Identifiers: chr22:g.50662837G>C (hg19) ; chr22:g.50224408G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50224408G>C , CM000684.2:g.50224408G>C	GRCh38
NC_000022.10:g.50662837G>C , CM000684.1:g.50662837G>C	GRCh37
NC_000022.9:g.49004964G>C	NCBI36
NG_032160.1:g.25564C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248846.10:c.2078C>G MANE Select	ENSP00000248846.5:p.Ser693Ter
ENST00000248846.9:c.2078C>G	ENSP00000248846.5:p.Ser693Ter
ENST00000439308.6:c.2078C>G	ENSP00000397387.2:p.Ser693Ter
ENST00000473946.1:n.387C>G
ENST00000489511.5:n.95C>G
ENST00000491449.5:n.385C>G
ENST00000498611.5:n.2611C>G
NM_020461.3:c.2078C>G	NP_065194.2:p.Ser693Ter
XR_938347.1:n.2643C>G
XR_938348.1:n.2643C>G
XR_001755343.2:n.2647C>G
XR_001755344.2:n.2647C>G
XR_002958720.1:n.2647C>G
XR_938347.2:n.2647C>G
NM_020461.4:c.2078C>G MANE Select	NP_065194.3:p.Ser693Ter