Canonical Allele Identifier: CA2410732535
Gene: TUBGCP6 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000022.11:g.50224365_50224367delinsCTG , CM000684.2:g.50224365_50224367delinsCTG GRCh38
NC_000022.10:g.50662794_50662796delinsCTG , CM000684.1:g.50662794_50662796delinsCTG GRCh37
NC_000022.9:g.49004921_49004923delinsCTG NCBI36
NG_032160.1:g.25605_25607delinsCAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000248846.10:c.2119_2121delinsCAG MANE Select ENSP00000248846.5:p.Gln707=
ENST00000248846.9:c.2119_2121delinsCAG ENSP00000248846.5:p.Gln707=
ENST00000439308.6:c.2119_2121delinsCAG ENSP00000397387.2:p.Gln707=
ENST00000473946.1:n.428_430delinsCAG
ENST00000489511.5:n.136_138delinsCAG
ENST00000491449.5:n.426_428delinsCAG
ENST00000498611.5:n.2652_2654delinsCAG
NM_020461.3:c.2119_2121delinsCAG NP_065194.2:p.Gln707=
XR_938347.1:n.2684_2686delinsCAG
XR_938348.1:n.2684_2686delinsCAG
XR_001755343.2:n.2688_2690delinsCAG
XR_001755344.2:n.2688_2690delinsCAG
XR_002958720.1:n.2688_2690delinsCAG
XR_938347.2:n.2688_2690delinsCAG
NM_020461.4:c.2119_2121delinsCAG MANE Select NP_065194.3:p.Gln707=
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