Canonical Allele Identifier: CA2035021858

Gene: TUBA1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185105C= , CM000674.2:g.49185105C=	GRCh38
NC_000012.11:g.49578888C= , CM000674.1:g.49578888C=	GRCh37
NC_000012.10:g.47865155C=	NCBI36
NG_008966.1:g.8974G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.1261G= MANE Select	ENSP00000301071.7:p.Ala421=
ENST00000547939.6:c.1156G=	ENSP00000450268.2:p.Ala386=
ENST00000550767.6:c.1156G=	ENSP00000446637.1:p.Ala386=
ENST00000550811.2:n.2294G=
ENST00000552924.2:c.1156G=	ENSP00000448725.2:p.Ala386=
ENST00000679733.1:c.*717G=	ENSP00000505459.1:n.*717G=
ENST00000295766.9:c.1261G=	ENSP00000439020.2:p.Ala421=
ENST00000301071.11:c.1261G=	ENSP00000301071.7:p.Ala421=
ENST00000550767.5:c.1156G=	ENSP00000446637.1:p.Ala386=
NM_001270399.1:c.1261G=	NP_001257328.1:p.Ala421=
NM_001270400.1:c.1156G=	NP_001257329.1:p.Ala386=
NM_006009.3:c.1261G=	NP_006000.2:p.Ala421=
NM_006009.4:c.1261G= MANE Select	NP_006000.2:p.Ala421=
NM_001270399.2:c.1261G=	NP_001257328.1:p.Ala421=
NM_001270400.2:c.1156G=	NP_001257329.1:p.Ala386=