Canonical Allele Identifier: CA509133406

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746291A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234923A>G , CM000681.2:g.57234923A>G	GRCh38
NC_000019.9:g.57746291A>G , CM000681.1:g.57746291A>G	GRCh37
NC_000019.8:g.62438103A>G	NCBI36
NG_012134.1:g.8915A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.624A>G MANE Select	ENSP00000302898.6:p.Pro208=
ENST00000302804.11:c.624A>G	ENSP00000302898.6:p.Pro208=
ENST00000415300.6:c.567A>G	ENSP00000407162.1:p.Pro189=
ENST00000448930.5:c.519A>G	ENSP00000406798.2:p.Pro173=
ENST00000594599.1:c.108A>G	ENSP00000469894.1:p.Pro36=
ENST00000596375.1:c.*185A>G	ENSP00000470465.1:n.*185A>G
ENST00000598785.5:c.522A>G	ENSP00000471830.1:p.Pro174=
ENST00000599062.5:c.615A>G	ENSP00000469983.1:p.Pro205=
ENST00000601799.5:c.*923A>G	ENSP00000468918.1:n.*923A>G
NM_001015878.1:c.624A>G	NP_001015878.1:p.Pro208=
NM_001015879.1:c.567A>G	NP_001015879.1:p.Pro189=
NM_003160.2:c.522A>G	NP_003151.2:p.Pro174=
XR_430209.2:n.1518A>G
XR_430209.3:n.1561A>G
NM_001015878.2:c.624A>G MANE Select	NP_001015878.1:p.Pro208=
NM_001015879.2:c.567A>G	NP_001015879.1:p.Pro189=
NM_003160.3:c.522A>G	NP_003151.2:p.Pro174=