Canonical Allele Identifier: CA407692549

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746266G>T (hg19) ; chr19:g.57234898G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234898G>T , CM000681.2:g.57234898G>T	GRCh38
NC_000019.9:g.57746266G>T , CM000681.1:g.57746266G>T	GRCh37
NC_000019.8:g.62438078G>T	NCBI36
NG_012134.1:g.8890G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.599G>T MANE Select	ENSP00000302898.6:p.Cys200Phe
ENST00000302804.11:c.599G>T	ENSP00000302898.6:p.Cys200Phe
ENST00000415300.6:c.542G>T	ENSP00000407162.1:p.Cys181Phe
ENST00000448930.5:c.494G>T	ENSP00000406798.2:p.Cys165Phe
ENST00000594599.1:c.83G>T	ENSP00000469894.1:p.Cys28Phe
ENST00000596375.1:c.*160G>T	ENSP00000470465.1:n.*160G>T
ENST00000598785.5:c.497G>T	ENSP00000471830.1:p.Cys166Phe
ENST00000599062.5:c.590G>T	ENSP00000469983.1:p.Cys197Phe
ENST00000601799.5:c.*898G>T	ENSP00000468918.1:n.*898G>T
NM_001015878.1:c.599G>T	NP_001015878.1:p.Cys200Phe
NM_001015879.1:c.542G>T	NP_001015879.1:p.Cys181Phe
NM_003160.2:c.497G>T	NP_003151.2:p.Cys166Phe
XR_430209.2:n.1493G>T
XR_430209.3:n.1536G>T
NM_001015878.2:c.599G>T MANE Select	NP_001015878.1:p.Cys200Phe
NM_001015879.2:c.542G>T	NP_001015879.1:p.Cys181Phe
NM_003160.3:c.497G>T	NP_003151.2:p.Cys166Phe