Canonical Allele Identifier: CA384642281

Gene: TUBA1A

Linked Data

• ClinVar Variation Id: 1304433
• ClinVar RCV Id: RCV001752200
• dbSNP Id: rs2121244807
• MyVariant Identifiers: chr12:g.49579664C>A (hg19) ; chr12:g.49185881C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185881C>A , CM000674.2:g.49185881C>A	GRCh38
NC_000012.11:g.49579664C>A , CM000674.1:g.49579664C>A	GRCh37
NC_000012.10:g.47865931C>A	NCBI36
NG_008966.1:g.8198G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.485G>T MANE Select	ENSP00000301071.7:p.Gly162Val
ENST00000547939.6:c.380G>T	ENSP00000450268.2:p.Gly127Val
ENST00000550767.6:c.380G>T	ENSP00000446637.1:p.Gly127Val
ENST00000550811.2:n.1518G>T
ENST00000552924.2:c.380G>T	ENSP00000448725.2:p.Gly127Val
ENST00000679733.1:c.508G>T	ENSP00000505459.1:p.Ala170Ser
ENST00000295766.9:c.485G>T	ENSP00000439020.2:p.Gly162Val
ENST00000301071.11:c.485G>T	ENSP00000301071.7:p.Gly162Val
ENST00000546918.1:c.637G>T	ENSP00000446613.1:p.Ala213Ser
ENST00000547939.5:c.380G>T	ENSP00000450268.1:p.Gly127Val
ENST00000550767.5:c.380G>T	ENSP00000446637.1:p.Gly127Val
NM_001270399.1:c.485G>T	NP_001257328.1:p.Gly162Val
NM_001270400.1:c.380G>T	NP_001257329.1:p.Gly127Val
NM_006009.3:c.485G>T	NP_006000.2:p.Gly162Val
NM_006009.4:c.485G>T MANE Select	NP_006000.2:p.Gly162Val
NM_001270399.2:c.485G>T	NP_001257328.1:p.Gly162Val
NM_001270400.2:c.380G>T	NP_001257329.1:p.Gly127Val