Canonical Allele Identifier: CA384642699

Gene: TUBA1A

Linked Data

• ClinVar Variation Id: 3236674
• ClinVar RCV Id: RCV004556134
• MyVariant Identifiers: chr12:g.49579728A>C (hg19) ; chr12:g.49185945A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185945A>C , CM000674.2:g.49185945A>C	GRCh38
NC_000012.11:g.49579728A>C , CM000674.1:g.49579728A>C	GRCh37
NC_000012.10:g.47865995A>C	NCBI36
NG_008966.1:g.8134T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.421T>G MANE Select	ENSP00000301071.7:p.Phe141Val
ENST00000547939.6:c.316T>G	ENSP00000450268.2:p.Phe106Val
ENST00000550767.6:c.316T>G	ENSP00000446637.1:p.Phe106Val
ENST00000550811.2:n.1454T>G
ENST00000552924.2:c.316T>G	ENSP00000448725.2:p.Phe106Val
ENST00000679733.1:c.444T>G	ENSP00000505459.1:p.Ala148=
ENST00000295766.9:c.421T>G	ENSP00000439020.2:p.Phe141Val
ENST00000301071.11:c.421T>G	ENSP00000301071.7:p.Phe141Val
ENST00000546918.1:c.573T>G	ENSP00000446613.1:p.Ala191=
ENST00000547939.5:c.316T>G	ENSP00000450268.1:p.Phe106Val
ENST00000550767.5:c.316T>G	ENSP00000446637.1:p.Phe106Val
ENST00000552924.1:c.316T>G	ENSP00000448725.1:p.Phe106Val
NM_001270399.1:c.421T>G	NP_001257328.1:p.Phe141Val
NM_001270400.1:c.316T>G	NP_001257329.1:p.Phe106Val
NM_006009.3:c.421T>G	NP_006000.2:p.Phe141Val
NM_006009.4:c.421T>G MANE Select	NP_006000.2:p.Phe141Val
NM_001270399.2:c.421T>G	NP_001257328.1:p.Phe141Val
NM_001270400.2:c.316T>G	NP_001257329.1:p.Phe106Val