Canonical Allele Identifier: CA515375947
Gene: TUBGCP6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.50659089A>T (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50220660A>T , CM000684.2:g.50220660A>T GRCh38
NC_000022.10:g.50659089A>T , CM000684.1:g.50659089A>T GRCh37
NC_000022.9:g.49001216A>T NCBI36
NG_032160.1:g.29312T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3699T>A MANE Select ENSP00000248846.5:p.Ala1233=
ENST00000248846.9:c.3699T>A ENSP00000248846.5:p.Ala1233=
ENST00000439308.6:c.3699T>A ENSP00000397387.2:p.Ala1233=
ENST00000491449.5:n.2006T>A
ENST00000498611.5:n.3617+615T>A
NM_020461.3:c.3699T>A NP_065194.2:p.Ala1233=
XR_938347.1:n.4264T>A
XR_938348.1:n.3050-645T>A
XR_001755343.2:n.4268T>A
XR_001755344.2:n.4268T>A
XR_002958720.1:n.3054-645T>A
XR_938347.2:n.4268T>A
NM_020461.4:c.3699T>A MANE Select NP_065194.3:p.Ala1233=