Canonical Allele Identifier: CA515376869

Gene: TUBGCP6

Linked Data

• MyVariant Identifiers: chr22:g.50662812C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50224383C>T , CM000684.2:g.50224383C>T	GRCh38
NC_000022.10:g.50662812C>T , CM000684.1:g.50662812C>T	GRCh37
NC_000022.9:g.49004939C>T	NCBI36
NG_032160.1:g.25589G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248846.10:c.2103G>A MANE Select	ENSP00000248846.5:p.Arg701=
ENST00000248846.9:c.2103G>A	ENSP00000248846.5:p.Arg701=
ENST00000439308.6:c.2103G>A	ENSP00000397387.2:p.Arg701=
ENST00000473946.1:n.412G>A
ENST00000489511.5:n.120G>A
ENST00000491449.5:n.410G>A
ENST00000498611.5:n.2636G>A
NM_020461.3:c.2103G>A	NP_065194.2:p.Arg701=
XR_938347.1:n.2668G>A
XR_938348.1:n.2668G>A
XR_001755343.2:n.2672G>A
XR_001755344.2:n.2672G>A
XR_002958720.1:n.2672G>A
XR_938347.2:n.2672G>A
NM_020461.4:c.2103G>A MANE Select	NP_065194.3:p.Arg701=