Canonical Allele Identifier: CA2035023072

Gene: TUBA1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185846C= , CM000674.2:g.49185846C=	GRCh38
NC_000012.11:g.49579629C= , CM000674.1:g.49579629C=	GRCh37
NC_000012.10:g.47865896C=	NCBI36
NG_008966.1:g.8233G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.520G= MANE Select	ENSP00000301071.7:p.Ala174=
ENST00000547939.6:c.415G=	ENSP00000450268.2:p.Ala139=
ENST00000550767.6:c.415G=	ENSP00000446637.1:p.Ala139=
ENST00000550811.2:n.1553G=
ENST00000552924.2:c.415G=	ENSP00000448725.2:p.Ala139=
ENST00000679733.1:c.543G=	ENSP00000505459.1:p.Arg181=
ENST00000295766.9:c.520G=	ENSP00000439020.2:p.Ala174=
ENST00000301071.11:c.520G=	ENSP00000301071.7:p.Ala174=
ENST00000546918.1:c.672G=	ENSP00000446613.1:p.Arg224=
ENST00000547939.5:c.415G=	ENSP00000450268.1:p.Ala139=
ENST00000550767.5:c.415G=	ENSP00000446637.1:p.Ala139=
NM_001270399.1:c.520G=	NP_001257328.1:p.Ala174=
NM_001270400.1:c.415G=	NP_001257329.1:p.Ala139=
NM_006009.3:c.520G=	NP_006000.2:p.Ala174=
NM_006009.4:c.520G= MANE Select	NP_006000.2:p.Ala174=
NM_001270399.2:c.520G=	NP_001257328.1:p.Ala174=
NM_001270400.2:c.415G=	NP_001257329.1:p.Ala139=