Canonical Allele Identifier: CA407692967

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746326T>C (hg19) ; chr19:g.57234958T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234958T>C , CM000681.2:g.57234958T>C	GRCh38
NC_000019.9:g.57746326T>C , CM000681.1:g.57746326T>C	GRCh37
NC_000019.8:g.62438138T>C	NCBI36
NG_012134.1:g.8950T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.659T>C MANE Select	ENSP00000302898.6:p.Val220Ala
ENST00000302804.11:c.659T>C	ENSP00000302898.6:p.Val220Ala
ENST00000415300.6:c.602T>C	ENSP00000407162.1:p.Val201Ala
ENST00000448930.5:c.554T>C	ENSP00000406798.2:p.Val185Ala
ENST00000594599.1:c.143T>C	ENSP00000469894.1:p.Val48Ala
ENST00000596375.1:c.*220T>C	ENSP00000470465.1:n.*220T>C
ENST00000598785.5:c.557T>C	ENSP00000471830.1:p.Val186Ala
ENST00000599062.5:c.650T>C	ENSP00000469983.1:p.Val217Ala
ENST00000601799.5:c.*958T>C	ENSP00000468918.1:n.*958T>C
NM_001015878.1:c.659T>C	NP_001015878.1:p.Val220Ala
NM_001015879.1:c.602T>C	NP_001015879.1:p.Val201Ala
NM_003160.2:c.557T>C	NP_003151.2:p.Val186Ala
XR_430209.2:n.1553T>C
XR_430209.3:n.1596T>C
NM_001015878.2:c.659T>C MANE Select	NP_001015878.1:p.Val220Ala
NM_001015879.2:c.602T>C	NP_001015879.1:p.Val201Ala
NM_003160.3:c.557T>C	NP_003151.2:p.Val186Ala