Canonical Allele Identifier: CA2035024314

Gene: TUBA1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49186800C= , CM000674.2:g.49186800C=	GRCh38
NC_000012.11:g.49580583C= , CM000674.1:g.49580583C=	GRCh37
NC_000012.10:g.47866850C=	NCBI36
NG_008966.1:g.7279G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.37G= MANE Select	ENSP00000301071.7:p.Gly13=
ENST00000547939.6:c.-69G=	ENSP00000450268.2:n.-69G=
ENST00000550767.6:c.-69G=	ENSP00000446637.1:n.-69G=
ENST00000550811.2:n.1070G=
ENST00000552924.2:c.-69G=	ENSP00000448725.2:n.-69G=
ENST00000679733.1:c.37G=	ENSP00000505459.1:p.Gly13=
ENST00000295766.9:c.37G=	ENSP00000439020.2:p.Gly13=
ENST00000301071.11:c.37G=	ENSP00000301071.7:p.Gly13=
ENST00000546918.1:c.37G=	ENSP00000446613.1:p.Gly13=
ENST00000547939.5:c.-69G=	ENSP00000450268.1:n.-69G=
ENST00000548363.1:n.41G=
ENST00000550254.1:n.59G=
ENST00000550767.5:c.-69G=	ENSP00000446637.1:n.-69G=
ENST00000550811.1:c.-69G=	ENSP00000449016.1:n.-69G=
ENST00000552924.1:c.-69G=	ENSP00000448725.1:n.-69G=
NM_001270399.1:c.37G=	NP_001257328.1:p.Gly13=
NM_001270400.1:c.-69G=	NP_001257329.1:n.-69G=
NM_006009.3:c.37G=	NP_006000.2:p.Gly13=
NM_006009.4:c.37G= MANE Select	NP_006000.2:p.Gly13=
NM_001270399.2:c.37G=	NP_001257328.1:p.Gly13=
NM_001270400.2:c.-69G=	NP_001257329.1:n.-69G=