Canonical Allele Identifier: CA2242020864
Gene: TUBB3 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.89935771_89935774delinsCGAG , CM000678.2:g.89935771_89935774delinsCGAG GRCh38
NC_000016.9:g.90002179_90002182delinsCGAG , CM000678.1:g.90002179_90002182delinsCGAG GRCh37
NC_000016.8:g.88529680_88529683delinsCGAG NCBI36
NG_027810.1:g.18763_18766delinsCGAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000315491.12:c.1320_1323delinsCGAG MANE Select ENSP00000320295.7:p.Asp440=
ENST00000680788.1:n.4741_4744delinsCGAG
ENST00000315491.11:c.1320_1323delinsCGAG ENSP00000320295.7:p.Asp440=
ENST00000554444.5:c.1104_1107delinsCGAG ENSP00000451617.1:p.Asp368=
ENST00000555576.5:c.277+2193_277+2196delinsCGAG ENSP00000452554.1:n.277+2193_277+2196delinsCGAG
ENST00000555609.5:c.*1405_*1408delinsCGAG ENSP00000451276.1:n.*1405_*1408delinsCGAG
ENST00000556922.1:c.2361_2364delinsCGAG ENSP00000451560.1:p.Asp787=
NM_001197181.1:c.1104_1107delinsCGAG NP_001184110.1:p.Asp368=
NM_006086.3:c.1320_1323delinsCGAG NP_006077.2:p.Asp440=
NM_006086.4:c.1320_1323delinsCGAG MANE Select NP_006077.2:p.Asp440=
NM_001197181.2:c.1104_1107delinsCGAG NP_001184110.1:p.Asp368=