Canonical Allele Identifier: CA407692514

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746262A>C (hg19) ; chr19:g.57234894A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234894A>C , CM000681.2:g.57234894A>C	GRCh38
NC_000019.9:g.57746262A>C , CM000681.1:g.57746262A>C	GRCh37
NC_000019.8:g.62438074A>C	NCBI36
NG_012134.1:g.8886A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.595A>C MANE Select	ENSP00000302898.6:p.Met199Leu
ENST00000302804.11:c.595A>C	ENSP00000302898.6:p.Met199Leu
ENST00000415300.6:c.538A>C	ENSP00000407162.1:p.Met180Leu
ENST00000448930.5:c.490A>C	ENSP00000406798.2:p.Met164Leu
ENST00000594599.1:c.79A>C	ENSP00000469894.1:p.Met27Leu
ENST00000596375.1:c.*156A>C	ENSP00000470465.1:n.*156A>C
ENST00000598785.5:c.493A>C	ENSP00000471830.1:p.Met165Leu
ENST00000599062.5:c.586A>C	ENSP00000469983.1:p.Met196Leu
ENST00000601799.5:c.*894A>C	ENSP00000468918.1:n.*894A>C
NM_001015878.1:c.595A>C	NP_001015878.1:p.Met199Leu
NM_001015879.1:c.538A>C	NP_001015879.1:p.Met180Leu
NM_003160.2:c.493A>C	NP_003151.2:p.Met165Leu
XR_430209.2:n.1489A>C
XR_430209.3:n.1532A>C
NM_001015878.2:c.595A>C MANE Select	NP_001015878.1:p.Met199Leu
NM_001015879.2:c.538A>C	NP_001015879.1:p.Met180Leu
NM_003160.3:c.493A>C	NP_003151.2:p.Met165Leu