Canonical Allele Identifier: CA384642631

Gene: TUBA1A

Linked Data

• gnomAD v4: 12-49185931-A-G
• MyVariant Identifiers: chr12:g.49579714A>G (hg19) ; chr12:g.49185931A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185931A>G , CM000674.2:g.49185931A>G	GRCh38
NC_000012.11:g.49579714A>G , CM000674.1:g.49579714A>G	GRCh37
NC_000012.10:g.47865981A>G	NCBI36
NG_008966.1:g.8148T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.435T>C MANE Select	ENSP00000301071.7:p.Thr145=
ENST00000547939.6:c.330T>C	ENSP00000450268.2:p.Thr110=
ENST00000550767.6:c.330T>C	ENSP00000446637.1:p.Thr110=
ENST00000550811.2:n.1468T>C
ENST00000552924.2:c.330T>C	ENSP00000448725.2:p.Thr110=
ENST00000679733.1:c.458T>C	ENSP00000505459.1:p.Leu153Pro
ENST00000295766.9:c.435T>C	ENSP00000439020.2:p.Thr145=
ENST00000301071.11:c.435T>C	ENSP00000301071.7:p.Thr145=
ENST00000546918.1:c.587T>C	ENSP00000446613.1:p.Leu196Pro
ENST00000547939.5:c.330T>C	ENSP00000450268.1:p.Thr110=
ENST00000550767.5:c.330T>C	ENSP00000446637.1:p.Thr110=
ENST00000552924.1:c.330T>C	ENSP00000448725.1:p.Thr110=
NM_001270399.1:c.435T>C	NP_001257328.1:p.Thr145=
NM_001270400.1:c.330T>C	NP_001257329.1:p.Thr110=
NM_006009.3:c.435T>C	NP_006000.2:p.Thr145=
NM_006009.4:c.435T>C MANE Select	NP_006000.2:p.Thr145=
NM_001270399.2:c.435T>C	NP_001257328.1:p.Thr145=
NM_001270400.2:c.330T>C	NP_001257329.1:p.Thr110=