Canonical Allele Identifier: CA407692973

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746328G>C (hg19) ; chr19:g.57234960G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234960G>C , CM000681.2:g.57234960G>C	GRCh38
NC_000019.9:g.57746328G>C , CM000681.1:g.57746328G>C	GRCh37
NC_000019.8:g.62438140G>C	NCBI36
NG_012134.1:g.8952G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.661G>C MANE Select	ENSP00000302898.6:p.Asp221His
ENST00000302804.11:c.661G>C	ENSP00000302898.6:p.Asp221His
ENST00000415300.6:c.604G>C	ENSP00000407162.1:p.Asp202His
ENST00000448930.5:c.556G>C	ENSP00000406798.2:p.Asp186His
ENST00000594599.1:c.145G>C	ENSP00000469894.1:p.Asp49His
ENST00000596375.1:c.*222G>C	ENSP00000470465.1:n.*222G>C
ENST00000598785.5:c.559G>C	ENSP00000471830.1:p.Asp187His
ENST00000599062.5:c.652G>C	ENSP00000469983.1:p.Asp218His
ENST00000601799.5:c.*960G>C	ENSP00000468918.1:n.*960G>C
NM_001015878.1:c.661G>C	NP_001015878.1:p.Asp221His
NM_001015879.1:c.604G>C	NP_001015879.1:p.Asp202His
NM_003160.2:c.559G>C	NP_003151.2:p.Asp187His
XR_430209.2:n.1555G>C
XR_430209.3:n.1598G>C
NM_001015878.2:c.661G>C MANE Select	NP_001015878.1:p.Asp221His
NM_001015879.2:c.604G>C	NP_001015879.1:p.Asp202His
NM_003160.3:c.559G>C	NP_003151.2:p.Asp187His