Canonical Allele Identifier: CA10652261

Gene: AURKC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57232596C>T , CM000681.2:g.57232596C>T	GRCh38
NC_000019.9:g.57743964C>T , CM000681.1:g.57743964C>T	GRCh37
NC_000019.8:g.62435776C>T	NCBI36
NG_012134.1:g.6588C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.351C>T MANE Select	ENSP00000302898.6:p.Tyr117=
ENST00000302804.11:c.351C>T	ENSP00000302898.6:p.Tyr117=
ENST00000415300.6:c.294C>T	ENSP00000407162.1:p.Tyr98=
ENST00000448930.5:c.249C>T	ENSP00000406798.2:p.Tyr83=
ENST00000596375.1:c.249C>T	ENSP00000470465.1:p.Tyr83=
ENST00000598785.5:c.249C>T	ENSP00000471830.1:p.Tyr83=
ENST00000599062.5:c.342C>T	ENSP00000469983.1:p.Tyr114=
ENST00000601799.5:c.*645C>T	ENSP00000468918.1:n.*645C>T
NM_001015878.1:c.351C>T	NP_001015878.1:p.Tyr117=
NM_001015879.1:c.294C>T	NP_001015879.1:p.Tyr98=
NM_003160.2:c.249C>T	NP_003151.2:p.Tyr83=
XR_430209.2:n.1240C>T
XR_430209.3:n.1283C>T
NM_001015878.2:c.351C>T MANE Select	NP_001015878.1:p.Tyr117=
NM_001015879.2:c.294C>T	NP_001015879.1:p.Tyr98=
NM_003160.3:c.249C>T	NP_003151.2:p.Tyr83=