Canonical Allele Identifier: CA9695857

Gene: AURKC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57231778G>T , CM000681.2:g.57231778G>T	GRCh38
NC_000019.9:g.57743146G>T , CM000681.1:g.57743146G>T	GRCh37
NC_000019.8:g.62434958G>T	NCBI36
NG_012134.1:g.5770G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.95G>T MANE Select	ENSP00000302898.6:p.Ser32Ile
ENST00000302804.11:c.95G>T	ENSP00000302898.6:p.Ser32Ile
ENST00000415300.6:c.38G>T	ENSP00000407162.1:p.Ser13Ile
ENST00000448930.5:c.-8G>T	ENSP00000406798.2:n.-8G>T
ENST00000596375.1:c.-8G>T	ENSP00000470465.1:n.-8G>T
ENST00000598785.5:c.-8G>T	ENSP00000471830.1:n.-8G>T
ENST00000599062.5:c.86G>T	ENSP00000469983.1:p.Ser29Ile
ENST00000601799.5:c.*389G>T	ENSP00000468918.1:n.*389G>T
NM_001015878.1:c.95G>T	NP_001015878.1:p.Ser32Ile
NM_001015879.1:c.38G>T	NP_001015879.1:p.Ser13Ile
NM_003160.2:c.-8G>T	NP_003151.2:n.-8G>T
XR_430209.2:n.984G>T
XR_430209.3:n.1027G>T
NM_001015878.2:c.95G>T MANE Select	NP_001015878.1:p.Ser32Ile
NM_001015879.2:c.38G>T	NP_001015879.1:p.Ser13Ile
NM_003160.3:c.-8G>T	NP_003151.2:n.-8G>T