Canonical Allele Identifier: CA407692764

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746294A>T (hg19) ; chr19:g.57234926A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234926A>T , CM000681.2:g.57234926A>T	GRCh38
NC_000019.9:g.57746294A>T , CM000681.1:g.57746294A>T	GRCh37
NC_000019.8:g.62438106A>T	NCBI36
NG_012134.1:g.8918A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.627A>T MANE Select	ENSP00000302898.6:p.Glu209Asp
ENST00000302804.11:c.627A>T	ENSP00000302898.6:p.Glu209Asp
ENST00000415300.6:c.570A>T	ENSP00000407162.1:p.Glu190Asp
ENST00000448930.5:c.522A>T	ENSP00000406798.2:p.Glu174Asp
ENST00000594599.1:c.111A>T	ENSP00000469894.1:p.Glu37Asp
ENST00000596375.1:c.*188A>T	ENSP00000470465.1:n.*188A>T
ENST00000598785.5:c.525A>T	ENSP00000471830.1:p.Glu175Asp
ENST00000599062.5:c.618A>T	ENSP00000469983.1:p.Glu206Asp
ENST00000601799.5:c.*926A>T	ENSP00000468918.1:n.*926A>T
NM_001015878.1:c.627A>T	NP_001015878.1:p.Glu209Asp
NM_001015879.1:c.570A>T	NP_001015879.1:p.Glu190Asp
NM_003160.2:c.525A>T	NP_003151.2:p.Glu175Asp
XR_430209.2:n.1521A>T
XR_430209.3:n.1564A>T
NM_001015878.2:c.627A>T MANE Select	NP_001015878.1:p.Glu209Asp
NM_001015879.2:c.570A>T	NP_001015879.1:p.Glu190Asp
NM_003160.3:c.525A>T	NP_003151.2:p.Glu175Asp