Canonical Allele Identifier: CA407692538

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746265T>C (hg19) ; chr19:g.57234897T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234897T>C , CM000681.2:g.57234897T>C	GRCh38
NC_000019.9:g.57746265T>C , CM000681.1:g.57746265T>C	GRCh37
NC_000019.8:g.62438077T>C	NCBI36
NG_012134.1:g.8889T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.598T>C MANE Select	ENSP00000302898.6:p.Cys200Arg
ENST00000302804.11:c.598T>C	ENSP00000302898.6:p.Cys200Arg
ENST00000415300.6:c.541T>C	ENSP00000407162.1:p.Cys181Arg
ENST00000448930.5:c.493T>C	ENSP00000406798.2:p.Cys165Arg
ENST00000594599.1:c.82T>C	ENSP00000469894.1:p.Cys28Arg
ENST00000596375.1:c.*159T>C	ENSP00000470465.1:n.*159T>C
ENST00000598785.5:c.496T>C	ENSP00000471830.1:p.Cys166Arg
ENST00000599062.5:c.589T>C	ENSP00000469983.1:p.Cys197Arg
ENST00000601799.5:c.*897T>C	ENSP00000468918.1:n.*897T>C
NM_001015878.1:c.598T>C	NP_001015878.1:p.Cys200Arg
NM_001015879.1:c.541T>C	NP_001015879.1:p.Cys181Arg
NM_003160.2:c.496T>C	NP_003151.2:p.Cys166Arg
XR_430209.2:n.1492T>C
XR_430209.3:n.1535T>C
NM_001015878.2:c.598T>C MANE Select	NP_001015878.1:p.Cys200Arg
NM_001015879.2:c.541T>C	NP_001015879.1:p.Cys181Arg
NM_003160.3:c.496T>C	NP_003151.2:p.Cys166Arg