Canonical Allele Identifier: CA515376408

Gene: TUBGCP6

Linked Data

• MyVariant Identifiers: chr22:g.50658885C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50220456C>G , CM000684.2:g.50220456C>G	GRCh38
NC_000022.10:g.50658885C>G , CM000684.1:g.50658885C>G	GRCh37
NC_000022.9:g.49001012C>G	NCBI36
NG_032160.1:g.29516G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248846.10:c.3903G>C MANE Select	ENSP00000248846.5:p.Thr1301=
ENST00000248846.9:c.3903G>C	ENSP00000248846.5:p.Thr1301=
ENST00000439308.6:c.3903G>C	ENSP00000397387.2:p.Thr1301=
ENST00000491449.5:n.2210G>C
ENST00000498611.5:n.3618-441G>C
NM_020461.3:c.3903G>C	NP_065194.2:p.Thr1301=
XR_938347.1:n.4468G>C
XR_938348.1:n.3050-441G>C
XR_001755343.2:n.4472G>C
XR_001755344.2:n.4472G>C
XR_002958720.1:n.3054-441G>C
XR_938347.2:n.4472G>C
NM_020461.4:c.3903G>C MANE Select	NP_065194.3:p.Thr1301=