Canonical Allele Identifier: CA479717181

Gene: TUBA1A

Linked Data

• MyVariant Identifiers: chr12:g.49579366G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185583G>C , CM000674.2:g.49185583G>C	GRCh38
NC_000012.11:g.49579366G>C , CM000674.1:g.49579366G>C	GRCh37
NC_000012.10:g.47865633G>C	NCBI36
NG_008966.1:g.8496C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000301071.12:c.783C>G MANE Select	ENSP00000301071.7:p.Pro261=
ENST00000547939.6:c.678C>G	ENSP00000450268.2:p.Pro226=
ENST00000550767.6:c.678C>G	ENSP00000446637.1:p.Pro226=
ENST00000550811.2:n.1816C>G
ENST00000552924.2:c.678C>G	ENSP00000448725.2:p.Pro226=
ENST00000679733.1:c.*239C>G	ENSP00000505459.1:n.*239C>G
ENST00000295766.9:c.783C>G	ENSP00000439020.2:p.Pro261=
ENST00000301071.11:c.783C>G	ENSP00000301071.7:p.Pro261=
ENST00000550767.5:c.678C>G	ENSP00000446637.1:p.Pro226=
NM_001270399.1:c.783C>G	NP_001257328.1:p.Pro261=
NM_001270400.1:c.678C>G	NP_001257329.1:p.Pro226=
NM_006009.3:c.783C>G	NP_006000.2:p.Pro261=
NM_006009.4:c.783C>G MANE Select	NP_006000.2:p.Pro261=
NM_001270399.2:c.783C>G	NP_001257328.1:p.Pro261=
NM_001270400.2:c.678C>G	NP_001257329.1:p.Pro226=