Canonical Allele Identifier: CA2035022210

Gene: TUBA1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185295G= , CM000674.2:g.49185295G=	GRCh38
NC_000012.11:g.49579078G= , CM000674.1:g.49579078G=	GRCh37
NC_000012.10:g.47865345G=	NCBI36
NG_008966.1:g.8784C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.1071C= MANE Select	ENSP00000301071.7:p.Tyr357=
ENST00000547939.6:c.966C=	ENSP00000450268.2:p.Tyr322=
ENST00000550767.6:c.966C=	ENSP00000446637.1:p.Tyr322=
ENST00000550811.2:n.2104C=
ENST00000552924.2:c.966C=	ENSP00000448725.2:p.Tyr322=
ENST00000679733.1:c.*527C=	ENSP00000505459.1:n.*527C=
ENST00000295766.9:c.1071C=	ENSP00000439020.2:p.Tyr357=
ENST00000301071.11:c.1071C=	ENSP00000301071.7:p.Tyr357=
ENST00000550767.5:c.966C=	ENSP00000446637.1:p.Tyr322=
NM_001270399.1:c.1071C=	NP_001257328.1:p.Tyr357=
NM_001270400.1:c.966C=	NP_001257329.1:p.Tyr322=
NM_006009.3:c.1071C=	NP_006000.2:p.Tyr357=
NM_006009.4:c.1071C= MANE Select	NP_006000.2:p.Tyr357=
NM_001270399.2:c.1071C=	NP_001257328.1:p.Tyr357=
NM_001270400.2:c.966C=	NP_001257329.1:p.Tyr322=