Canonical Allele Identifier: CA407692443

Gene: AURKC

Linked Data

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

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.586A>T MANE Select	ENSP00000302898.6:p.Arg196Trp
ENST00000302804.11:c.586A>T	ENSP00000302898.6:p.Arg196Trp
ENST00000415300.6:c.529A>T	ENSP00000407162.1:p.Arg177Trp
ENST00000448930.5:c.481A>T	ENSP00000406798.2:p.Arg161Trp
ENST00000594599.1:c.70A>T	ENSP00000469894.1:p.Arg24Trp
ENST00000596375.1:c.*147A>T	ENSP00000470465.1:n.*147A>T
ENST00000598785.5:c.484A>T	ENSP00000471830.1:p.Arg162Trp
ENST00000599062.5:c.577A>T	ENSP00000469983.1:p.Arg193Trp
ENST00000601799.5:c.*885A>T	ENSP00000468918.1:n.*885A>T
NM_001015878.1:c.586A>T	NP_001015878.1:p.Arg196Trp
NM_001015879.1:c.529A>T	NP_001015879.1:p.Arg177Trp
NM_003160.2:c.484A>T	NP_003151.2:p.Arg162Trp
XR_430209.2:n.1480A>T
XR_430209.3:n.1523A>T
NM_001015878.2:c.586A>T MANE Select	NP_001015878.1:p.Arg196Trp
NM_001015879.2:c.529A>T	NP_001015879.1:p.Arg177Trp
NM_003160.3:c.484A>T	NP_003151.2:p.Arg162Trp