Canonical Allele Identifier: CA9696044

Gene: AURKC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57235043C>G , CM000681.2:g.57235043C>G	GRCh38
NC_000019.9:g.57746411C>G , CM000681.1:g.57746411C>G	GRCh37
NC_000019.8:g.62438223C>G	NCBI36
NG_012134.1:g.9035C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.744C>G MANE Select	ENSP00000302898.6:p.Tyr248Ter
ENST00000302804.11:c.744C>G	ENSP00000302898.6:p.Tyr248Ter
ENST00000415300.6:c.687C>G	ENSP00000407162.1:p.Tyr229Ter
ENST00000448930.5:c.639C>G	ENSP00000406798.2:p.Tyr213Ter
ENST00000594599.1:c.228C>G	ENSP00000469894.1:p.Tyr76Ter
ENST00000596375.1:c.*305C>G	ENSP00000470465.1:n.*305C>G
ENST00000598785.5:c.642C>G	ENSP00000471830.1:p.Tyr214Ter
ENST00000599062.5:c.735C>G	ENSP00000469983.1:p.Tyr245Ter
ENST00000601799.5:c.*1043C>G	ENSP00000468918.1:n.*1043C>G
NM_001015878.1:c.744C>G	NP_001015878.1:p.Tyr248Ter
NM_001015879.1:c.687C>G	NP_001015879.1:p.Tyr229Ter
NM_003160.2:c.642C>G	NP_003151.2:p.Tyr214Ter
XR_430209.2:n.1638C>G
XR_430209.3:n.1681C>G
NM_001015878.2:c.744C>G MANE Select	NP_001015878.1:p.Tyr248Ter
NM_001015879.2:c.687C>G	NP_001015879.1:p.Tyr229Ter
NM_003160.3:c.642C>G	NP_003151.2:p.Tyr214Ter