Canonical Allele Identifier: CA9695805

Gene: AURKC

Linked Data

• ClinVar Variation Id: 330226
• ClinVar RCV Id: RCV000311416 ; RCV001707654
• dbSNP Id: rs74179426
• ExAC: 19:57742514 G / GC
• gnomAD v2: 19-57742514-G-GC
• gnomAD v3: 19-57231146-G-GC
• gnomAD v4: 19-57231146-G-GC
• COSMIC: COSN20116142
• MyVariant Identifiers: chr19:g.57742518dupC (hg19) ; chr19:g.57742514_57742515insC (hg19) ; chr19:g.57231150dupC (hg38) ; chr19:g.57231146_57231147insC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57231150dup , CM000681.2:g.57231150dup	GRCh38
NC_000019.9:g.57742518dup , CM000681.1:g.57742518dup	GRCh37
NC_000019.8:g.62434330dup	NCBI36
NG_012134.1:g.5142dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.-99dup MANE Select	ENSP00000302898.6:n.-99dup
ENST00000302804.11:c.-99dup	ENSP00000302898.6:n.-99dup
ENST00000415300.6:c.1+36dup	ENSP00000407162.1:n.1+36dup
ENST00000448930.5:c.-45+30dup	ENSP00000406798.2:n.-45+30dup
ENST00000601799.5:c.-99dup	ENSP00000468918.1:n.-99dup
NM_001015878.1:c.-99dup	NP_001015878.1:n.-99dup
NM_001015879.1:c.1+36dup	NP_001015879.1:n.1+36dup
NM_003160.2:c.-45+31dup	NP_003151.2:n.-45+31dup
XR_430209.2:n.791dup
XR_430209.3:n.834dup
NM_001015878.2:c.-99dup MANE Select	NP_001015878.1:n.-99dup
NM_001015879.2:c.1+36dup	NP_001015879.1:n.1+36dup
NM_003160.3:c.-45+31dup	NP_003151.2:n.-45+31dup