Canonical Allele Identifier: CA407692527

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746263T>G (hg19) ; chr19:g.57234895T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234895T>G , CM000681.2:g.57234895T>G	GRCh38
NC_000019.9:g.57746263T>G , CM000681.1:g.57746263T>G	GRCh37
NC_000019.8:g.62438075T>G	NCBI36
NG_012134.1:g.8887T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.596T>G MANE Select	ENSP00000302898.6:p.Met199Arg
ENST00000302804.11:c.596T>G	ENSP00000302898.6:p.Met199Arg
ENST00000415300.6:c.539T>G	ENSP00000407162.1:p.Met180Arg
ENST00000448930.5:c.491T>G	ENSP00000406798.2:p.Met164Arg
ENST00000594599.1:c.80T>G	ENSP00000469894.1:p.Met27Arg
ENST00000596375.1:c.*157T>G	ENSP00000470465.1:n.*157T>G
ENST00000598785.5:c.494T>G	ENSP00000471830.1:p.Met165Arg
ENST00000599062.5:c.587T>G	ENSP00000469983.1:p.Met196Arg
ENST00000601799.5:c.*895T>G	ENSP00000468918.1:n.*895T>G
NM_001015878.1:c.596T>G	NP_001015878.1:p.Met199Arg
NM_001015879.1:c.539T>G	NP_001015879.1:p.Met180Arg
NM_003160.2:c.494T>G	NP_003151.2:p.Met165Arg
XR_430209.2:n.1490T>G
XR_430209.3:n.1533T>G
NM_001015878.2:c.596T>G MANE Select	NP_001015878.1:p.Met199Arg
NM_001015879.2:c.539T>G	NP_001015879.1:p.Met180Arg
NM_003160.3:c.494T>G	NP_003151.2:p.Met165Arg