Canonical Allele Identifier: CA384639744

Gene: TUBA1A

Linked Data

• MyVariant Identifiers: chr12:g.49579362G>C (hg19) ; chr12:g.49185579G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185579G>C , CM000674.2:g.49185579G>C	GRCh38
NC_000012.11:g.49579362G>C , CM000674.1:g.49579362G>C	GRCh37
NC_000012.10:g.47865629G>C	NCBI36
NG_008966.1:g.8500C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000301071.12:c.787C>G MANE Select	ENSP00000301071.7:p.Pro263Ala
ENST00000547939.6:c.682C>G	ENSP00000450268.2:p.Pro228Ala
ENST00000550767.6:c.682C>G	ENSP00000446637.1:p.Pro228Ala
ENST00000550811.2:n.1820C>G
ENST00000552924.2:c.682C>G	ENSP00000448725.2:p.Pro228Ala
ENST00000679733.1:c.*243C>G	ENSP00000505459.1:n.*243C>G
ENST00000295766.9:c.787C>G	ENSP00000439020.2:p.Pro263Ala
ENST00000301071.11:c.787C>G	ENSP00000301071.7:p.Pro263Ala
ENST00000550767.5:c.682C>G	ENSP00000446637.1:p.Pro228Ala
NM_001270399.1:c.787C>G	NP_001257328.1:p.Pro263Ala
NM_001270400.1:c.682C>G	NP_001257329.1:p.Pro228Ala
NM_006009.3:c.787C>G	NP_006000.2:p.Pro263Ala
NM_006009.4:c.787C>G MANE Select	NP_006000.2:p.Pro263Ala
NM_001270399.2:c.787C>G	NP_001257328.1:p.Pro263Ala
NM_001270400.2:c.682C>G	NP_001257329.1:p.Pro228Ala