Canonical Allele Identifier: CA515377018

Gene: TUBGCP6

Linked Data

• MyVariant Identifiers: chr22:g.50659530G>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50221101G>T , CM000684.2:g.50221101G>T	GRCh38
NC_000022.10:g.50659530G>T , CM000684.1:g.50659530G>T	GRCh37
NC_000022.9:g.49001657G>T	NCBI36
NG_032160.1:g.28871C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248846.10:c.3258C>A MANE Select	ENSP00000248846.5:p.Ala1086=
ENST00000248846.9:c.3258C>A	ENSP00000248846.5:p.Ala1086=
ENST00000439308.6:c.3258C>A	ENSP00000397387.2:p.Ala1086=
ENST00000491449.5:n.1565C>A
ENST00000498611.5:n.3617+174C>A
NM_020461.3:c.3258C>A	NP_065194.2:p.Ala1086=
XR_938347.1:n.3823C>A
XR_938348.1:n.3049+927C>A
XR_001755343.2:n.3827C>A
XR_001755344.2:n.3827C>A
XR_002958720.1:n.3053+927C>A
XR_938347.2:n.3827C>A
NM_020461.4:c.3258C>A MANE Select	NP_065194.3:p.Ala1086=