Canonical Allele Identifier: CA1884919041

Gene: TUBB8

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.48779G= , CM000672.2:g.48779G=	GRCh38
NC_000010.10:g.94719G= , CM000672.1:g.94719G=	GRCh37
NC_000010.9:g.84719G=	NCBI36
NG_046777.1:g.32677C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000568584.6:c.166+25C= MANE Select	ENSP00000456206.2:n.166+25C=
ENST00000561967.1:c.166+25C=	ENSP00000454878.1:n.166+25C=
ENST00000562809.1:c.58-54C=	ENSP00000456899.1:n.58-54C=
ENST00000563456.1:n.222C=
ENST00000564130.2:c.115C=	ENSP00000457610.1:p.Arg39=
ENST00000567466.1:c.90+25C=	ENSP00000454914.1:n.90+25C=
ENST00000568584.5:c.166+25C=	ENSP00000456206.1:n.166+25C=
ENST00000568866.5:c.166+25C=	ENSP00000457062.1:n.166+25C=
NM_177987.2:c.166+25C=	NP_817124.1:n.166+25C=
XM_011519458.1:c.-51+25C=	XP_011517760.1:n.-51+25C=
XM_011519459.1:c.-51+25C=	XP_011517761.1:n.-51+25C=
XM_011519459.3:c.-51+25C=	XP_011517761.1:n.-51+25C=
NM_177987.3:c.166+25C= MANE Select	NP_817124.1:n.166+25C=
NM_001389618.1:c.-51+25C=	NP_001376547.1:n.-51+25C=
NM_001389619.1:c.-51+25C=	NP_001376548.1:n.-51+25C=