Canonical Allele Identifier: CA407692441

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746253A>G (hg19) ; chr19:g.57234885A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234885A>G , CM000681.2:g.57234885A>G	GRCh38
NC_000019.9:g.57746253A>G , CM000681.1:g.57746253A>G	GRCh37
NC_000019.8:g.62438065A>G	NCBI36
NG_012134.1:g.8877A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.586A>G MANE Select	ENSP00000302898.6:p.Arg196Gly
ENST00000302804.11:c.586A>G	ENSP00000302898.6:p.Arg196Gly
ENST00000415300.6:c.529A>G	ENSP00000407162.1:p.Arg177Gly
ENST00000448930.5:c.481A>G	ENSP00000406798.2:p.Arg161Gly
ENST00000594599.1:c.70A>G	ENSP00000469894.1:p.Arg24Gly
ENST00000596375.1:c.*147A>G	ENSP00000470465.1:n.*147A>G
ENST00000598785.5:c.484A>G	ENSP00000471830.1:p.Arg162Gly
ENST00000599062.5:c.577A>G	ENSP00000469983.1:p.Arg193Gly
ENST00000601799.5:c.*885A>G	ENSP00000468918.1:n.*885A>G
NM_001015878.1:c.586A>G	NP_001015878.1:p.Arg196Gly
NM_001015879.1:c.529A>G	NP_001015879.1:p.Arg177Gly
NM_003160.2:c.484A>G	NP_003151.2:p.Arg162Gly
XR_430209.2:n.1480A>G
XR_430209.3:n.1523A>G
NM_001015878.2:c.586A>G MANE Select	NP_001015878.1:p.Arg196Gly
NM_001015879.2:c.529A>G	NP_001015879.1:p.Arg177Gly
NM_003160.3:c.484A>G	NP_003151.2:p.Arg162Gly