Canonical Allele Identifier: CA2242021080
Gene: TUBB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89935905_89935906delinsCT , CM000678.2:g.89935905_89935906delinsCT GRCh38
NC_000016.9:g.90002313_90002314delinsCT , CM000678.1:g.90002313_90002314delinsCT GRCh37
NC_000016.8:g.88529814_88529815delinsCT NCBI36
NG_027810.1:g.18897_18898delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000315491.12:c.*101_*102delinsCT MANE Select ENSP00000320295.7:n.*101_*102delinsCT
ENST00000680788.1:n.4875_4876delinsCT
ENST00000315491.11:c.*101_*102delinsCT ENSP00000320295.7:n.*101_*102delinsCT
ENST00000554444.5:c.*101_*102delinsCT ENSP00000451617.1:n.*101_*102delinsCT
ENST00000555576.5:c.277+2327_277+2328delinsCT ENSP00000452554.1:n.277+2327_277+2328delinsCT
ENST00000555609.5:c.*1539_*1540delinsCT ENSP00000451276.1:n.*1539_*1540delinsCT
ENST00000556922.1:c.*101_*102delinsCT ENSP00000451560.1:n.*101_*102delinsCT
NM_001197181.1:c.*101_*102delinsCT NP_001184110.1:n.*101_*102delinsCT
NM_006086.3:c.*101_*102delinsCT NP_006077.2:n.*101_*102delinsCT
NM_006086.4:c.*101_*102delinsCT MANE Select NP_006077.2:n.*101_*102delinsCT
NM_001197181.2:c.*101_*102delinsCT NP_001184110.1:n.*101_*102delinsCT