Canonical Allele Identifier: CA236622617

Gene: TUBA1A

Linked Data

• ClinVar Variation Id: 2895251
• ClinVar RCV Id: RCV003728332
• dbSNP Id: rs544713824
• gnomAD v2: 12-49579606-T-C
• gnomAD v3: 12-49185823-T-C
• gnomAD v4: 12-49185823-T-C
• MyVariant Identifiers: chr12:g.49579606T>C (hg19) ; chr12:g.49185823T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185823T>C , CM000674.2:g.49185823T>C	GRCh38
NC_000012.11:g.49579606T>C , CM000674.1:g.49579606T>C	GRCh37
NC_000012.10:g.47865873T>C	NCBI36
NG_008966.1:g.8256A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.543A>G MANE Select	ENSP00000301071.7:p.Val181=
ENST00000547939.6:c.438A>G	ENSP00000450268.2:p.Val146=
ENST00000550767.6:c.438A>G	ENSP00000446637.1:p.Val146=
ENST00000550811.2:n.1576A>G
ENST00000552924.2:c.438A>G	ENSP00000448725.2:p.Val146=
ENST00000679733.1:c.566A>G	ENSP00000505459.1:p.Ter189Trp
ENST00000295766.9:c.543A>G	ENSP00000439020.2:p.Val181=
ENST00000301071.11:c.543A>G	ENSP00000301071.7:p.Val181=
ENST00000546918.1:c.695A>G	ENSP00000446613.1:p.Ter232Trp
ENST00000547939.5:c.438A>G	ENSP00000450268.1:p.Val146=
ENST00000550767.5:c.438A>G	ENSP00000446637.1:p.Val146=
NM_001270399.1:c.543A>G	NP_001257328.1:p.Val181=
NM_001270400.1:c.438A>G	NP_001257329.1:p.Val146=
NM_006009.3:c.543A>G	NP_006000.2:p.Val181=
NM_006009.4:c.543A>G MANE Select	NP_006000.2:p.Val181=
NM_001270399.2:c.543A>G	NP_001257328.1:p.Val181=
NM_001270400.2:c.438A>G	NP_001257329.1:p.Val146=