Canonical Allele Identifier: CA412178090

Gene: TUBGCP6

Linked Data

• ClinVar Variation Id: 1033534
• ClinVar RCV Id: RCV001335973
• dbSNP Id: rs2064499588
• MyVariant Identifiers: chr22:g.50658920T>G (hg19) ; chr22:g.50220491T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50220491T>G , CM000684.2:g.50220491T>G	GRCh38
NC_000022.10:g.50658920T>G , CM000684.1:g.50658920T>G	GRCh37
NC_000022.9:g.49001047T>G	NCBI36
NG_032160.1:g.29481A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248846.10:c.3868A>C MANE Select	ENSP00000248846.5:p.Thr1290Pro
ENST00000248846.9:c.3868A>C	ENSP00000248846.5:p.Thr1290Pro
ENST00000439308.6:c.3868A>C	ENSP00000397387.2:p.Thr1290Pro
ENST00000491449.5:n.2175A>C
ENST00000498611.5:n.3618-476A>C
NM_020461.3:c.3868A>C	NP_065194.2:p.Thr1290Pro
XR_938347.1:n.4433A>C
XR_938348.1:n.3050-476A>C
XR_001755343.2:n.4437A>C
XR_001755344.2:n.4437A>C
XR_002958720.1:n.3054-476A>C
XR_938347.2:n.4437A>C
NM_020461.4:c.3868A>C MANE Select	NP_065194.3:p.Thr1290Pro