Canonical Allele Identifier: CA407692554

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746267T>G (hg19) ; chr19:g.57234899T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234899T>G , CM000681.2:g.57234899T>G	GRCh38
NC_000019.9:g.57746267T>G , CM000681.1:g.57746267T>G	GRCh37
NC_000019.8:g.62438079T>G	NCBI36
NG_012134.1:g.8891T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.600T>G MANE Select	ENSP00000302898.6:p.Cys200Trp
ENST00000302804.11:c.600T>G	ENSP00000302898.6:p.Cys200Trp
ENST00000415300.6:c.543T>G	ENSP00000407162.1:p.Cys181Trp
ENST00000448930.5:c.495T>G	ENSP00000406798.2:p.Cys165Trp
ENST00000594599.1:c.84T>G	ENSP00000469894.1:p.Cys28Trp
ENST00000596375.1:c.*161T>G	ENSP00000470465.1:n.*161T>G
ENST00000598785.5:c.498T>G	ENSP00000471830.1:p.Cys166Trp
ENST00000599062.5:c.591T>G	ENSP00000469983.1:p.Cys197Trp
ENST00000601799.5:c.*899T>G	ENSP00000468918.1:n.*899T>G
NM_001015878.1:c.600T>G	NP_001015878.1:p.Cys200Trp
NM_001015879.1:c.543T>G	NP_001015879.1:p.Cys181Trp
NM_003160.2:c.498T>G	NP_003151.2:p.Cys166Trp
XR_430209.2:n.1494T>G
XR_430209.3:n.1537T>G
NM_001015878.2:c.600T>G MANE Select	NP_001015878.1:p.Cys200Trp
NM_001015879.2:c.543T>G	NP_001015879.1:p.Cys181Trp
NM_003160.3:c.498T>G	NP_003151.2:p.Cys166Trp