Canonical Allele Identifier: CA515376258

Gene: TUBGCP6

Linked Data

• MyVariant Identifiers: chr22:g.50659191C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50220762C>T , CM000684.2:g.50220762C>T	GRCh38
NC_000022.10:g.50659191C>T , CM000684.1:g.50659191C>T	GRCh37
NC_000022.9:g.49001318C>T	NCBI36
NG_032160.1:g.29210G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248846.10:c.3597G>A MANE Select	ENSP00000248846.5:p.Gly1199=
ENST00000248846.9:c.3597G>A	ENSP00000248846.5:p.Gly1199=
ENST00000439308.6:c.3597G>A	ENSP00000397387.2:p.Gly1199=
ENST00000491449.5:n.1904G>A
ENST00000498611.5:n.3617+513G>A
NM_020461.3:c.3597G>A	NP_065194.2:p.Gly1199=
XR_938347.1:n.4162G>A
XR_938348.1:n.3050-747G>A
XR_001755343.2:n.4166G>A
XR_001755344.2:n.4166G>A
XR_002958720.1:n.3054-747G>A
XR_938347.2:n.4166G>A
NM_020461.4:c.3597G>A MANE Select	NP_065194.3:p.Gly1199=