Canonical Allele Identifier: CA515376666
Gene: TUBGCP6 HGNC NCBI

Linked Data

MyVariant Identifiers: chr22:g.50658936T>A (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50220507T>A , CM000684.2:g.50220507T>A GRCh38
NC_000022.10:g.50658936T>A , CM000684.1:g.50658936T>A GRCh37
NC_000022.9:g.49001063T>A NCBI36
NG_032160.1:g.29465A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.3852A>T MANE Select ENSP00000248846.5:p.Pro1284=
ENST00000248846.9:c.3852A>T ENSP00000248846.5:p.Pro1284=
ENST00000439308.6:c.3852A>T ENSP00000397387.2:p.Pro1284=
ENST00000491449.5:n.2159A>T
ENST00000498611.5:n.3618-492A>T
NM_020461.3:c.3852A>T NP_065194.2:p.Pro1284=
XR_938347.1:n.4417A>T
XR_938348.1:n.3050-492A>T
XR_001755343.2:n.4421A>T
XR_001755344.2:n.4421A>T
XR_002958720.1:n.3054-492A>T
XR_938347.2:n.4421A>T
NM_020461.4:c.3852A>T MANE Select NP_065194.3:p.Pro1284=