Canonical Allele Identifier: CA9696031

Gene: AURKC

Linked Data

• dbSNP Id: rs749429409
• ExAC: 19:57746333 G / A
• gnomAD v2: 19-57746333-G-A
• MyVariant Identifiers: chr19:g.57746333G>A (hg19) ; chr19:g.57234965G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234965G>A , CM000681.2:g.57234965G>A	GRCh38
NC_000019.9:g.57746333G>A , CM000681.1:g.57746333G>A	GRCh37
NC_000019.8:g.62438145G>A	NCBI36
NG_012134.1:g.8957G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.666G>A MANE Select	ENSP00000302898.6:p.Leu222=
ENST00000302804.11:c.666G>A	ENSP00000302898.6:p.Leu222=
ENST00000415300.6:c.609G>A	ENSP00000407162.1:p.Leu203=
ENST00000448930.5:c.561G>A	ENSP00000406798.2:p.Leu187=
ENST00000594599.1:c.150G>A	ENSP00000469894.1:p.Leu50=
ENST00000596375.1:c.*227G>A	ENSP00000470465.1:n.*227G>A
ENST00000598785.5:c.564G>A	ENSP00000471830.1:p.Leu188=
ENST00000599062.5:c.657G>A	ENSP00000469983.1:p.Leu219=
ENST00000601799.5:c.*965G>A	ENSP00000468918.1:n.*965G>A
NM_001015878.1:c.666G>A	NP_001015878.1:p.Leu222=
NM_001015879.1:c.609G>A	NP_001015879.1:p.Leu203=
NM_003160.2:c.564G>A	NP_003151.2:p.Leu188=
XR_430209.2:n.1560G>A
XR_430209.3:n.1603G>A
NM_001015878.2:c.666G>A MANE Select	NP_001015878.1:p.Leu222=
NM_001015879.2:c.609G>A	NP_001015879.1:p.Leu203=
NM_003160.3:c.564G>A	NP_003151.2:p.Leu188=