Canonical Allele Identifier: CA2035024194

Gene: TUBA1A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49186685G= , CM000674.2:g.49186685G=	GRCh38
NC_000012.11:g.49580468G= , CM000674.1:g.49580468G=	GRCh37
NC_000012.10:g.47866735G=	NCBI36
NG_008966.1:g.7394C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.152C= MANE Select	ENSP00000301071.7:p.Thr51=
ENST00000547939.6:c.47C=	ENSP00000450268.2:p.Thr16=
ENST00000550767.6:c.47C=	ENSP00000446637.1:p.Thr16=
ENST00000550811.2:n.1185C=
ENST00000552924.2:c.47C=	ENSP00000448725.2:p.Thr16=
ENST00000679733.1:c.152C=	ENSP00000505459.1:p.Thr51=
ENST00000295766.9:c.152C=	ENSP00000439020.2:p.Thr51=
ENST00000301071.11:c.152C=	ENSP00000301071.7:p.Thr51=
ENST00000546918.1:c.152C=	ENSP00000446613.1:p.Thr51=
ENST00000547939.5:c.47C=	ENSP00000450268.1:p.Thr16=
ENST00000548363.1:n.156C=
ENST00000550254.1:n.174C=
ENST00000550767.5:c.47C=	ENSP00000446637.1:p.Thr16=
ENST00000550811.1:c.47C=	ENSP00000449016.1:p.Thr16=
ENST00000552924.1:c.47C=	ENSP00000448725.1:p.Thr16=
NM_001270399.1:c.152C=	NP_001257328.1:p.Thr51=
NM_001270400.1:c.47C=	NP_001257329.1:p.Thr16=
NM_006009.3:c.152C=	NP_006000.2:p.Thr51=
NM_006009.4:c.152C= MANE Select	NP_006000.2:p.Thr51=
NM_001270399.2:c.152C=	NP_001257328.1:p.Thr51=
NM_001270400.2:c.47C=	NP_001257329.1:p.Thr16=