Canonical Allele Identifier: CA479717640
Gene: TUBA1A HGNC NCBI

Linked Data

MyVariant Identifiers: chr12:g.49580533G>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49186750G>C , CM000674.2:g.49186750G>C GRCh38
NC_000012.11:g.49580533G>C , CM000674.1:g.49580533G>C GRCh37
NC_000012.10:g.47866800G>C NCBI36
NG_008966.1:g.7329C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000301071.12:c.87C>G MANE Select ENSP00000301071.7:p.Gly29=
ENST00000547939.6:c.-19C>G ENSP00000450268.2:n.-19C>G
ENST00000550767.6:c.-19C>G ENSP00000446637.1:n.-19C>G
ENST00000550811.2:n.1120C>G
ENST00000552924.2:c.-19C>G ENSP00000448725.2:n.-19C>G
ENST00000679733.1:c.87C>G ENSP00000505459.1:p.Gly29=
ENST00000295766.9:c.87C>G ENSP00000439020.2:p.Gly29=
ENST00000301071.11:c.87C>G ENSP00000301071.7:p.Gly29=
ENST00000546918.1:c.87C>G ENSP00000446613.1:p.Gly29=
ENST00000547939.5:c.-19C>G ENSP00000450268.1:n.-19C>G
ENST00000548363.1:n.91C>G
ENST00000550254.1:n.109C>G
ENST00000550767.5:c.-19C>G ENSP00000446637.1:n.-19C>G
ENST00000550811.1:c.-19C>G ENSP00000449016.1:n.-19C>G
ENST00000552924.1:c.-19C>G ENSP00000448725.1:n.-19C>G
NM_001270399.1:c.87C>G NP_001257328.1:p.Gly29=
NM_001270400.1:c.-19C>G NP_001257329.1:n.-19C>G
NM_006009.3:c.87C>G NP_006000.2:p.Gly29=
NM_006009.4:c.87C>G MANE Select NP_006000.2:p.Gly29=
NM_001270399.2:c.87C>G NP_001257328.1:p.Gly29=
NM_001270400.2:c.-19C>G NP_001257329.1:n.-19C>G