Canonical Allele Identifier: CA407693082

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746350T>G (hg19) ; chr19:g.57234982T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234982T>G , CM000681.2:g.57234982T>G	GRCh38
NC_000019.9:g.57746350T>G , CM000681.1:g.57746350T>G	GRCh37
NC_000019.8:g.62438162T>G	NCBI36
NG_012134.1:g.8974T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.683T>G MANE Select	ENSP00000302898.6:p.Leu228Arg
ENST00000302804.11:c.683T>G	ENSP00000302898.6:p.Leu228Arg
ENST00000415300.6:c.626T>G	ENSP00000407162.1:p.Leu209Arg
ENST00000448930.5:c.578T>G	ENSP00000406798.2:p.Leu193Arg
ENST00000594599.1:c.167T>G	ENSP00000469894.1:p.Leu56Arg
ENST00000596375.1:c.*244T>G	ENSP00000470465.1:n.*244T>G
ENST00000598785.5:c.581T>G	ENSP00000471830.1:p.Leu194Arg
ENST00000599062.5:c.674T>G	ENSP00000469983.1:p.Leu225Arg
ENST00000601799.5:c.*982T>G	ENSP00000468918.1:n.*982T>G
NM_001015878.1:c.683T>G	NP_001015878.1:p.Leu228Arg
NM_001015879.1:c.626T>G	NP_001015879.1:p.Leu209Arg
NM_003160.2:c.581T>G	NP_003151.2:p.Leu194Arg
XR_430209.2:n.1577T>G
XR_430209.3:n.1620T>G
NM_001015878.2:c.683T>G MANE Select	NP_001015878.1:p.Leu228Arg
NM_001015879.2:c.626T>G	NP_001015879.1:p.Leu209Arg
NM_003160.3:c.581T>G	NP_003151.2:p.Leu194Arg