Canonical Allele Identifier: CA407692498

Gene: AURKC

Linked Data

• COSMIC: COSM714232 ; COSM714233
• MyVariant Identifiers: chr19:g.57746259A>G (hg19) ; chr19:g.57234891A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234891A>G , CM000681.2:g.57234891A>G	GRCh38
NC_000019.9:g.57746259A>G , CM000681.1:g.57746259A>G	GRCh37
NC_000019.8:g.62438071A>G	NCBI36
NG_012134.1:g.8883A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.592A>G MANE Select	ENSP00000302898.6:p.Thr198Ala
ENST00000302804.11:c.592A>G	ENSP00000302898.6:p.Thr198Ala
ENST00000415300.6:c.535A>G	ENSP00000407162.1:p.Thr179Ala
ENST00000448930.5:c.487A>G	ENSP00000406798.2:p.Thr163Ala
ENST00000594599.1:c.76A>G	ENSP00000469894.1:p.Thr26Ala
ENST00000596375.1:c.*153A>G	ENSP00000470465.1:n.*153A>G
ENST00000598785.5:c.490A>G	ENSP00000471830.1:p.Thr164Ala
ENST00000599062.5:c.583A>G	ENSP00000469983.1:p.Thr195Ala
ENST00000601799.5:c.*891A>G	ENSP00000468918.1:n.*891A>G
NM_001015878.1:c.592A>G	NP_001015878.1:p.Thr198Ala
NM_001015879.1:c.535A>G	NP_001015879.1:p.Thr179Ala
NM_003160.2:c.490A>G	NP_003151.2:p.Thr164Ala
XR_430209.2:n.1486A>G
XR_430209.3:n.1529A>G
NM_001015878.2:c.592A>G MANE Select	NP_001015878.1:p.Thr198Ala
NM_001015879.2:c.535A>G	NP_001015879.1:p.Thr179Ala
NM_003160.3:c.490A>G	NP_003151.2:p.Thr164Ala