Canonical Allele Identifier: CA384639641

Gene: TUBA1A

Linked Data

• COSMIC: COSM4961324
• MyVariant Identifiers: chr12:g.49579347G>A (hg19) ; chr12:g.49185564G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.49185564G>A , CM000674.2:g.49185564G>A	GRCh38
NC_000012.11:g.49579347G>A , CM000674.1:g.49579347G>A	GRCh37
NC_000012.10:g.47865614G>A	NCBI36
NG_008966.1:g.8515C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000301071.12:c.802C>T MANE Select	ENSP00000301071.7:p.Pro268Ser
ENST00000547939.6:c.697C>T	ENSP00000450268.2:p.Pro233Ser
ENST00000550767.6:c.697C>T	ENSP00000446637.1:p.Pro233Ser
ENST00000550811.2:n.1835C>T
ENST00000552924.2:c.697C>T	ENSP00000448725.2:p.Pro233Ser
ENST00000679733.1:c.*258C>T	ENSP00000505459.1:n.*258C>T
ENST00000295766.9:c.802C>T	ENSP00000439020.2:p.Pro268Ser
ENST00000301071.11:c.802C>T	ENSP00000301071.7:p.Pro268Ser
ENST00000550767.5:c.697C>T	ENSP00000446637.1:p.Pro233Ser
NM_001270399.1:c.802C>T	NP_001257328.1:p.Pro268Ser
NM_001270400.1:c.697C>T	NP_001257329.1:p.Pro233Ser
NM_006009.3:c.802C>T	NP_006000.2:p.Pro268Ser
NM_006009.4:c.802C>T MANE Select	NP_006000.2:p.Pro268Ser
NM_001270399.2:c.802C>T	NP_001257328.1:p.Pro268Ser
NM_001270400.2:c.697C>T	NP_001257329.1:p.Pro233Ser