Canonical Allele Identifier: CA384642848

Gene: TUBA1A

Linked Data

• gnomAD v4: 12-49185976-C-A
• MyVariant Identifiers: chr12:g.49579759C>A (hg19) ; chr12:g.49185976C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185976C>A , CM000674.2:g.49185976C>A	GRCh38
NC_000012.11:g.49579759C>A , CM000674.1:g.49579759C>A	GRCh37
NC_000012.10:g.47866026C>A	NCBI36
NG_008966.1:g.8103G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.390G>T MANE Select	ENSP00000301071.7:p.Thr130=
ENST00000547939.6:c.285G>T	ENSP00000450268.2:p.Thr95=
ENST00000550767.6:c.285G>T	ENSP00000446637.1:p.Thr95=
ENST00000550811.2:n.1423G>T
ENST00000552924.2:c.285G>T	ENSP00000448725.2:p.Thr95=
ENST00000679733.1:c.413G>T	ENSP00000505459.1:p.Arg138Leu
ENST00000295766.9:c.390G>T	ENSP00000439020.2:p.Thr130=
ENST00000301071.11:c.390G>T	ENSP00000301071.7:p.Thr130=
ENST00000546918.1:c.542G>T	ENSP00000446613.1:p.Arg181Leu
ENST00000547939.5:c.285G>T	ENSP00000450268.1:p.Thr95=
ENST00000550767.5:c.285G>T	ENSP00000446637.1:p.Thr95=
ENST00000552924.1:c.285G>T	ENSP00000448725.1:p.Thr95=
NM_001270399.1:c.390G>T	NP_001257328.1:p.Thr130=
NM_001270400.1:c.285G>T	NP_001257329.1:p.Thr95=
NM_006009.3:c.390G>T	NP_006000.2:p.Thr130=
NM_006009.4:c.390G>T MANE Select	NP_006000.2:p.Thr130=
NM_001270399.2:c.390G>T	NP_001257328.1:p.Thr130=
NM_001270400.2:c.285G>T	NP_001257329.1:p.Thr95=