Canonical Allele Identifier: CA384638403

Gene: TUBA1A

Linked Data

• ClinVar Variation Id: 431850
• ClinVar RCV Id: RCV000497595 ; RCV000767448
• dbSNP Id: rs1555162327
• MyVariant Identifiers: chr12:g.49579230G>A (hg19) ; chr12:g.49185447G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185447G>A , CM000674.2:g.49185447G>A	GRCh38
NC_000012.11:g.49579230G>A , CM000674.1:g.49579230G>A	GRCh37
NC_000012.10:g.47865497G>A	NCBI36
NG_008966.1:g.8632C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.919C>T MANE Select	ENSP00000301071.7:p.Pro307Ser
ENST00000547939.6:c.814C>T	ENSP00000450268.2:p.Pro272Ser
ENST00000550767.6:c.814C>T	ENSP00000446637.1:p.Pro272Ser
ENST00000550811.2:n.1952C>T
ENST00000552924.2:c.814C>T	ENSP00000448725.2:p.Pro272Ser
ENST00000679733.1:c.*375C>T	ENSP00000505459.1:n.*375C>T
ENST00000295766.9:c.919C>T	ENSP00000439020.2:p.Pro307Ser
ENST00000301071.11:c.919C>T	ENSP00000301071.7:p.Pro307Ser
ENST00000550767.5:c.814C>T	ENSP00000446637.1:p.Pro272Ser
NM_001270399.1:c.919C>T	NP_001257328.1:p.Pro307Ser
NM_001270400.1:c.814C>T	NP_001257329.1:p.Pro272Ser
NM_006009.3:c.919C>T	NP_006000.2:p.Pro307Ser
NM_006009.4:c.919C>T MANE Select	NP_006000.2:p.Pro307Ser
NM_001270399.2:c.919C>T	NP_001257328.1:p.Pro307Ser
NM_001270400.2:c.814C>T	NP_001257329.1:p.Pro272Ser