Canonical Allele Identifier: CA515376287
Gene: TUBGCP6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.50658858T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50220429T>A , CM000684.2:g.50220429T>A GRCh38
NC_000022.10:g.50658858T>A , CM000684.1:g.50658858T>A GRCh37
NC_000022.9:g.49000985T>A NCBI36
NG_032160.1:g.29543A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3930A>T MANE Select ENSP00000248846.5:p.Ala1310=
ENST00000248846.9:c.3930A>T ENSP00000248846.5:p.Ala1310=
ENST00000439308.6:c.3930A>T ENSP00000397387.2:p.Ala1310=
ENST00000491449.5:n.2237A>T
ENST00000498611.5:n.3618-414A>T
NM_020461.3:c.3930A>T NP_065194.2:p.Ala1310=
XR_938347.1:n.4495A>T
XR_938348.1:n.3050-414A>T
XR_001755343.2:n.4499A>T
XR_001755344.2:n.4499A>T
XR_002958720.1:n.3054-414A>T
XR_938347.2:n.4499A>T
NM_020461.4:c.3930A>T MANE Select NP_065194.3:p.Ala1310=