Canonical Allele Identifier: CA2035023186

Gene: TUBA1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185942C= , CM000674.2:g.49185942C=	GRCh38
NC_000012.11:g.49579725C= , CM000674.1:g.49579725C=	GRCh37
NC_000012.10:g.47865992C=	NCBI36
NG_008966.1:g.8137G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.424G= MANE Select	ENSP00000301071.7:p.Gly142=
ENST00000547939.6:c.319G=	ENSP00000450268.2:p.Gly107=
ENST00000550767.6:c.319G=	ENSP00000446637.1:p.Gly107=
ENST00000550811.2:n.1457G=
ENST00000552924.2:c.319G=	ENSP00000448725.2:p.Gly107=
ENST00000679733.1:c.447G=	ENSP00000505459.1:p.Leu149=
ENST00000295766.9:c.424G=	ENSP00000439020.2:p.Gly142=
ENST00000301071.11:c.424G=	ENSP00000301071.7:p.Gly142=
ENST00000546918.1:c.576G=	ENSP00000446613.1:p.Leu192=
ENST00000547939.5:c.319G=	ENSP00000450268.1:p.Gly107=
ENST00000550767.5:c.319G=	ENSP00000446637.1:p.Gly107=
ENST00000552924.1:c.319G=	ENSP00000448725.1:p.Gly107=
NM_001270399.1:c.424G=	NP_001257328.1:p.Gly142=
NM_001270400.1:c.319G=	NP_001257329.1:p.Gly107=
NM_006009.3:c.424G=	NP_006000.2:p.Gly142=
NM_006009.4:c.424G= MANE Select	NP_006000.2:p.Gly142=
NM_001270399.2:c.424G=	NP_001257328.1:p.Gly142=
NM_001270400.2:c.319G=	NP_001257329.1:p.Gly107=