Canonical Allele Identifier: CA407688569

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57742482A>C (hg19) ; chr19:g.57231114A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57231114A>C , CM000681.2:g.57231114A>C	GRCh38
NC_000019.9:g.57742482A>C , CM000681.1:g.57742482A>C	GRCh37
NC_000019.8:g.62434294A>C	NCBI36
NG_012134.1:g.5106A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.-135A>C MANE Select	ENSP00000302898.6:n.-135A>C
ENST00000302804.11:c.-135A>C	ENSP00000302898.6:n.-135A>C
ENST00000415300.6:c.1A>C	ENSP00000407162.1:p.Met1Leu
ENST00000448930.5:c.-51A>C	ENSP00000406798.2:n.-51A>C
NM_001015878.1:c.-135A>C	NP_001015878.1:n.-135A>C
NM_001015879.1:c.1A>C	NP_001015879.1:p.Met1Leu
NM_003160.2:c.-50A>C	NP_003151.2:n.-50A>C
XR_430209.2:n.755A>C
XR_430209.3:n.798A>C
NM_001015878.2:c.-135A>C MANE Select	NP_001015878.1:n.-135A>C
NM_001015879.2:c.1A>C	NP_001015879.1:p.Met1Leu
NM_003160.3:c.-50A>C	NP_003151.2:n.-50A>C