Canonical Allele Identifier: CA407692958

Gene: AURKC

Linked Data

• ClinVar Variation Id: 2238742
• ClinVar RCV Id: RCV002737125
• gnomAD v4: 19-57234957-G-A
• MyVariant Identifiers: chr19:g.57746325G>A (hg19) ; chr19:g.57234957G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234957G>A , CM000681.2:g.57234957G>A	GRCh38
NC_000019.9:g.57746325G>A , CM000681.1:g.57746325G>A	GRCh37
NC_000019.8:g.62438137G>A	NCBI36
NG_012134.1:g.8949G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.658G>A MANE Select	ENSP00000302898.6:p.Val220Met
ENST00000302804.11:c.658G>A	ENSP00000302898.6:p.Val220Met
ENST00000415300.6:c.601G>A	ENSP00000407162.1:p.Val201Met
ENST00000448930.5:c.553G>A	ENSP00000406798.2:p.Val185Met
ENST00000594599.1:c.142G>A	ENSP00000469894.1:p.Val48Met
ENST00000596375.1:c.*219G>A	ENSP00000470465.1:n.*219G>A
ENST00000598785.5:c.556G>A	ENSP00000471830.1:p.Val186Met
ENST00000599062.5:c.649G>A	ENSP00000469983.1:p.Val217Met
ENST00000601799.5:c.*957G>A	ENSP00000468918.1:n.*957G>A
NM_001015878.1:c.658G>A	NP_001015878.1:p.Val220Met
NM_001015879.1:c.601G>A	NP_001015879.1:p.Val201Met
NM_003160.2:c.556G>A	NP_003151.2:p.Val186Met
XR_430209.2:n.1552G>A
XR_430209.3:n.1595G>A
NM_001015878.2:c.658G>A MANE Select	NP_001015878.1:p.Val220Met
NM_001015879.2:c.601G>A	NP_001015879.1:p.Val201Met
NM_003160.3:c.556G>A	NP_003151.2:p.Val186Met