Canonical Allele Identifier: CA515376626

Gene: TUBGCP6

Linked Data

• MyVariant Identifiers: chr22:g.50659725G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000022.11:g.50221296G>C , CM000684.2:g.50221296G>C	GRCh38
NC_000022.10:g.50659725G>C , CM000684.1:g.50659725G>C	GRCh37
NC_000022.9:g.49001852G>C	NCBI36
NG_032160.1:g.28676C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000248846.10:c.3063C>G MANE Select	ENSP00000248846.5:p.Pro1021=
ENST00000248846.9:c.3063C>G	ENSP00000248846.5:p.Pro1021=
ENST00000439308.6:c.3063C>G	ENSP00000397387.2:p.Pro1021=
ENST00000491449.5:n.1370C>G
ENST00000498611.5:n.3596C>G
NM_020461.3:c.3063C>G	NP_065194.2:p.Pro1021=
XR_938347.1:n.3628C>G
XR_938348.1:n.3049+732C>G
XR_001755343.2:n.3632C>G
XR_001755344.2:n.3632C>G
XR_002958720.1:n.3053+732C>G
XR_938347.2:n.3632C>G
NM_020461.4:c.3063C>G MANE Select	NP_065194.3:p.Pro1021=