Canonical Allele Identifier: CA204630
Gene: TUBA1A HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.49186832C>T , CM000674.2:g.49186832C>T GRCh38
NC_000012.11:g.49580615C>T , CM000674.1:g.49580615C>T GRCh37
NC_000012.10:g.47866882C>T NCBI36
NG_008966.1:g.7247G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000301071.12:c.5G>A MANE Select ENSP00000301071.7:p.Arg2His
ENST00000547939.6:c.-101G>A ENSP00000450268.2:n.-101G>A
ENST00000550767.6:c.-101G>A ENSP00000446637.1:n.-101G>A
ENST00000550811.2:n.1038G>A
ENST00000552924.2:c.-101G>A ENSP00000448725.2:n.-101G>A
ENST00000679733.1:c.5G>A ENSP00000505459.1:p.Arg2His
ENST00000295766.9:c.5G>A ENSP00000439020.2:p.Arg2His
ENST00000301071.11:c.5G>A ENSP00000301071.7:p.Arg2His
ENST00000546918.1:c.5G>A ENSP00000446613.1:p.Arg2His
ENST00000547939.5:c.-101G>A ENSP00000450268.1:n.-101G>A
ENST00000548363.1:n.9G>A
ENST00000550254.1:n.27G>A
ENST00000550767.5:c.-101G>A ENSP00000446637.1:n.-101G>A
ENST00000550811.1:c.-101G>A ENSP00000449016.1:n.-101G>A
ENST00000552924.1:c.-101G>A ENSP00000448725.1:n.-101G>A
NM_001270399.1:c.5G>A NP_001257328.1:p.Arg2His
NM_001270400.1:c.-101G>A NP_001257329.1:n.-101G>A
NM_006009.3:c.5G>A NP_006000.2:p.Arg2His
NM_006009.4:c.5G>A MANE Select NP_006000.2:p.Arg2His
NM_001270399.2:c.5G>A NP_001257328.1:p.Arg2His
NM_001270400.2:c.-101G>A NP_001257329.1:n.-101G>A