Canonical Allele Identifier: CA407692978

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746329A>C (hg19) ; chr19:g.57234961A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234961A>C , CM000681.2:g.57234961A>C	GRCh38
NC_000019.9:g.57746329A>C , CM000681.1:g.57746329A>C	GRCh37
NC_000019.8:g.62438141A>C	NCBI36
NG_012134.1:g.8953A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.662A>C MANE Select	ENSP00000302898.6:p.Asp221Ala
ENST00000302804.11:c.662A>C	ENSP00000302898.6:p.Asp221Ala
ENST00000415300.6:c.605A>C	ENSP00000407162.1:p.Asp202Ala
ENST00000448930.5:c.557A>C	ENSP00000406798.2:p.Asp186Ala
ENST00000594599.1:c.146A>C	ENSP00000469894.1:p.Asp49Ala
ENST00000596375.1:c.*223A>C	ENSP00000470465.1:n.*223A>C
ENST00000598785.5:c.560A>C	ENSP00000471830.1:p.Asp187Ala
ENST00000599062.5:c.653A>C	ENSP00000469983.1:p.Asp218Ala
ENST00000601799.5:c.*961A>C	ENSP00000468918.1:n.*961A>C
NM_001015878.1:c.662A>C	NP_001015878.1:p.Asp221Ala
NM_001015879.1:c.605A>C	NP_001015879.1:p.Asp202Ala
NM_003160.2:c.560A>C	NP_003151.2:p.Asp187Ala
XR_430209.2:n.1556A>C
XR_430209.3:n.1599A>C
NM_001015878.2:c.662A>C MANE Select	NP_001015878.1:p.Asp221Ala
NM_001015879.2:c.605A>C	NP_001015879.1:p.Asp202Ala
NM_003160.3:c.560A>C	NP_003151.2:p.Asp187Ala