Canonical Allele Identifier: CA2635070972

Gene: TUBB3

Linked Data

• gnomAD v4: 16-89935901-T-TCC

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.89935904_89935905dup , CM000678.2:g.89935904_89935905dup	GRCh38
NC_000016.9:g.90002312_90002313dup , CM000678.1:g.90002312_90002313dup	GRCh37
NC_000016.8:g.88529813_88529814dup	NCBI36
NG_027810.1:g.18896_18897dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000315491.12:c.*100_*101dup MANE Select	ENSP00000320295.7:n.*100_*101dup
ENST00000680788.1:n.4874_4875dup
ENST00000315491.11:c.*100_*101dup	ENSP00000320295.7:n.*100_*101dup
ENST00000554444.5:c.*100_*101dup	ENSP00000451617.1:n.*100_*101dup
ENST00000555576.5:c.277+2326_277+2327dup	ENSP00000452554.1:n.277+2326_277+2327dup
ENST00000555609.5:c.*1538_*1539dup	ENSP00000451276.1:n.*1538_*1539dup
ENST00000556922.1:c.*100_*101dup	ENSP00000451560.1:n.*100_*101dup
NM_001197181.1:c.*100_*101dup	NP_001184110.1:n.*100_*101dup
NM_006086.3:c.*100_*101dup	NP_006077.2:n.*100_*101dup
NM_006086.4:c.*100_*101dup MANE Select	NP_006077.2:n.*100_*101dup
NM_001197181.2:c.*100_*101dup	NP_001184110.1:n.*100_*101dup