Canonical Allele Identifier: CA6550236

Gene: TUBA1A

Linked Data

• ClinVar Variation Id: 1926079
• ClinVar RCV Id: RCV002605022
• dbSNP Id: rs777403500
• ExAC: 12:49579519 A / G
• gnomAD v2: 12-49579519-A-G
• gnomAD v3: 12-49185736-A-G
• gnomAD v4: 12-49185736-A-G
• MyVariant Identifiers: chr12:g.49579519A>G (hg19) ; chr12:g.49185736A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185736A>G , CM000674.2:g.49185736A>G	GRCh38
NC_000012.11:g.49579519A>G , CM000674.1:g.49579519A>G	GRCh37
NC_000012.10:g.47865786A>G	NCBI36
NG_008966.1:g.8343T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.630T>C MANE Select	ENSP00000301071.7:p.Tyr210=
ENST00000547939.6:c.525T>C	ENSP00000450268.2:p.Tyr175=
ENST00000550767.6:c.525T>C	ENSP00000446637.1:p.Tyr175=
ENST00000550811.2:n.1663T>C
ENST00000552924.2:c.525T>C	ENSP00000448725.2:p.Tyr175=
ENST00000679733.1:c.*86T>C	ENSP00000505459.1:n.*86T>C
ENST00000295766.9:c.630T>C	ENSP00000439020.2:p.Tyr210=
ENST00000301071.11:c.630T>C	ENSP00000301071.7:p.Tyr210=
ENST00000546918.1:c.*86T>C	ENSP00000446613.1:n.*86T>C
ENST00000547939.5:c.525T>C	ENSP00000450268.1:p.Tyr175=
ENST00000550767.5:c.525T>C	ENSP00000446637.1:p.Tyr175=
NM_001270399.1:c.630T>C	NP_001257328.1:p.Tyr210=
NM_001270400.1:c.525T>C	NP_001257329.1:p.Tyr175=
NM_006009.3:c.630T>C	NP_006000.2:p.Tyr210=
NM_006009.4:c.630T>C MANE Select	NP_006000.2:p.Tyr210=
NM_001270399.2:c.630T>C	NP_001257328.1:p.Tyr210=
NM_001270400.2:c.525T>C	NP_001257329.1:p.Tyr175=