Canonical Allele Identifier: CA384641841

Gene: TUBA1A

Linked Data

• MyVariant Identifiers: chr12:g.49579604A>T (hg19) ; chr12:g.49185821A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185821A>T , CM000674.2:g.49185821A>T	GRCh38
NC_000012.11:g.49579604A>T , CM000674.1:g.49579604A>T	GRCh37
NC_000012.10:g.47865871A>T	NCBI36
NG_008966.1:g.8258T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.545T>A MANE Select	ENSP00000301071.7:p.Val182Asp
ENST00000547939.6:c.440T>A	ENSP00000450268.2:p.Val147Asp
ENST00000550767.6:c.440T>A	ENSP00000446637.1:p.Val147Asp
ENST00000550811.2:n.1578T>A
ENST00000552924.2:c.440T>A	ENSP00000448725.2:p.Val147Asp
ENST00000679733.1:c.*1T>A	ENSP00000505459.1:n.*1T>A
ENST00000295766.9:c.545T>A	ENSP00000439020.2:p.Val182Asp
ENST00000301071.11:c.545T>A	ENSP00000301071.7:p.Val182Asp
ENST00000546918.1:c.*1T>A	ENSP00000446613.1:n.*1T>A
ENST00000547939.5:c.440T>A	ENSP00000450268.1:p.Val147Asp
ENST00000550767.5:c.440T>A	ENSP00000446637.1:p.Val147Asp
NM_001270399.1:c.545T>A	NP_001257328.1:p.Val182Asp
NM_001270400.1:c.440T>A	NP_001257329.1:p.Val147Asp
NM_006009.3:c.545T>A	NP_006000.2:p.Val182Asp
NM_006009.4:c.545T>A MANE Select	NP_006000.2:p.Val182Asp
NM_001270399.2:c.545T>A	NP_001257328.1:p.Val182Asp
NM_001270400.2:c.440T>A	NP_001257329.1:p.Val147Asp