Canonical Allele Identifier: CA9695984

Gene: AURKC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57233456A>G , CM000681.2:g.57233456A>G	GRCh38
NC_000019.9:g.57744824A>G , CM000681.1:g.57744824A>G	GRCh37
NC_000019.8:g.62436636A>G	NCBI36
NG_012134.1:g.7448A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.436-4A>G MANE Select	ENSP00000302898.6:n.436-4A>G
ENST00000302804.11:c.436-4A>G	ENSP00000302898.6:n.436-4A>G
ENST00000415300.6:c.379-4A>G	ENSP00000407162.1:n.379-4A>G
ENST00000448930.5:c.334-4A>G	ENSP00000406798.2:n.334-4A>G
ENST00000594599.1:c.68+771A>G	ENSP00000469894.1:n.68+771A>G
ENST00000596375.1:c.339-4A>G	ENSP00000470465.1:n.339-4A>G
ENST00000598785.5:c.334-4A>G	ENSP00000471830.1:n.334-4A>G
ENST00000599062.5:c.427-4A>G	ENSP00000469983.1:n.427-4A>G
ENST00000601799.5:c.*735-4A>G	ENSP00000468918.1:n.*735-4A>G
NM_001015878.1:c.436-4A>G	NP_001015878.1:n.436-4A>G
NM_001015879.1:c.379-4A>G	NP_001015879.1:n.379-4A>G
NM_003160.2:c.334-4A>G	NP_003151.2:n.334-4A>G
XR_430209.2:n.1330-4A>G
XR_430209.3:n.1373-4A>G
NM_001015878.2:c.436-4A>G MANE Select	NP_001015878.1:n.436-4A>G
NM_001015879.2:c.379-4A>G	NP_001015879.1:n.379-4A>G
NM_003160.3:c.334-4A>G	NP_003151.2:n.334-4A>G