Canonical Allele Identifier: CA479717395

Gene: TUBA1A

Linked Data

• MyVariant Identifiers: chr12:g.49579483T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185700T>A , CM000674.2:g.49185700T>A	GRCh38
NC_000012.11:g.49579483T>A , CM000674.1:g.49579483T>A	GRCh37
NC_000012.10:g.47865750T>A	NCBI36
NG_008966.1:g.8379A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.666A>T MANE Select	ENSP00000301071.7:p.Pro222=
ENST00000547939.6:c.561A>T	ENSP00000450268.2:p.Pro187=
ENST00000550767.6:c.561A>T	ENSP00000446637.1:p.Pro187=
ENST00000550811.2:n.1699A>T
ENST00000552924.2:c.561A>T	ENSP00000448725.2:p.Pro187=
ENST00000679733.1:c.*122A>T	ENSP00000505459.1:n.*122A>T
ENST00000295766.9:c.666A>T	ENSP00000439020.2:p.Pro222=
ENST00000301071.11:c.666A>T	ENSP00000301071.7:p.Pro222=
ENST00000546918.1:c.*122A>T	ENSP00000446613.1:n.*122A>T
ENST00000547939.5:c.561A>T	ENSP00000450268.1:p.Pro187=
ENST00000550767.5:c.561A>T	ENSP00000446637.1:p.Pro187=
NM_001270399.1:c.666A>T	NP_001257328.1:p.Pro222=
NM_001270400.1:c.561A>T	NP_001257329.1:p.Pro187=
NM_006009.3:c.666A>T	NP_006000.2:p.Pro222=
NM_006009.4:c.666A>T MANE Select	NP_006000.2:p.Pro222=
NM_001270399.2:c.666A>T	NP_001257328.1:p.Pro222=
NM_001270400.2:c.561A>T	NP_001257329.1:p.Pro187=