Canonical Allele Identifier: CA407692846

Gene: AURKC

Linked Data

• dbSNP Id: rs1568484991
• gnomAD v4: 19-57234936-G-A
• MyVariant Identifiers: chr19:g.57746304G>A (hg19) ; chr19:g.57234936G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234936G>A , CM000681.2:g.57234936G>A	GRCh38
NC_000019.9:g.57746304G>A , CM000681.1:g.57746304G>A	GRCh37
NC_000019.8:g.62438116G>A	NCBI36
NG_012134.1:g.8928G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.637G>A MANE Select	ENSP00000302898.6:p.Gly213Arg
ENST00000302804.11:c.637G>A	ENSP00000302898.6:p.Gly213Arg
ENST00000415300.6:c.580G>A	ENSP00000407162.1:p.Gly194Arg
ENST00000448930.5:c.532G>A	ENSP00000406798.2:p.Gly178Arg
ENST00000594599.1:c.121G>A	ENSP00000469894.1:p.Gly41Arg
ENST00000596375.1:c.*198G>A	ENSP00000470465.1:n.*198G>A
ENST00000598785.5:c.535G>A	ENSP00000471830.1:p.Gly179Arg
ENST00000599062.5:c.628G>A	ENSP00000469983.1:p.Gly210Arg
ENST00000601799.5:c.*936G>A	ENSP00000468918.1:n.*936G>A
NM_001015878.1:c.637G>A	NP_001015878.1:p.Gly213Arg
NM_001015879.1:c.580G>A	NP_001015879.1:p.Gly194Arg
NM_003160.2:c.535G>A	NP_003151.2:p.Gly179Arg
XR_430209.2:n.1531G>A
XR_430209.3:n.1574G>A
NM_001015878.2:c.637G>A MANE Select	NP_001015878.1:p.Gly213Arg
NM_001015879.2:c.580G>A	NP_001015879.1:p.Gly194Arg
NM_003160.3:c.535G>A	NP_003151.2:p.Gly179Arg