Canonical Allele Identifier: CA412177969

Gene: TUBGCP6

Linked Data

• ClinVar Variation Id: 546025
• ClinVar RCV Id: RCV000657781
• dbSNP Id: rs1555907270
• MyVariant Identifiers: chr22:g.50658905G>A (hg19) ; chr22:g.50220476G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50220476G>A , CM000684.2:g.50220476G>A	GRCh38
NC_000022.10:g.50658905G>A , CM000684.1:g.50658905G>A	GRCh37
NC_000022.9:g.49001032G>A	NCBI36
NG_032160.1:g.29496C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248846.10:c.3883C>T MANE Select	ENSP00000248846.5:p.Gln1295Ter
ENST00000248846.9:c.3883C>T	ENSP00000248846.5:p.Gln1295Ter
ENST00000439308.6:c.3883C>T	ENSP00000397387.2:p.Gln1295Ter
ENST00000491449.5:n.2190C>T
ENST00000498611.5:n.3618-461C>T
NM_020461.3:c.3883C>T	NP_065194.2:p.Gln1295Ter
XR_938347.1:n.4448C>T
XR_938348.1:n.3050-461C>T
XR_001755343.2:n.4452C>T
XR_001755344.2:n.4452C>T
XR_002958720.1:n.3054-461C>T
XR_938347.2:n.4452C>T
NM_020461.4:c.3883C>T MANE Select	NP_065194.3:p.Gln1295Ter