Canonical Allele Identifier: CA407693032

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746340A>G (hg19) ; chr19:g.57234972A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234972A>G , CM000681.2:g.57234972A>G	GRCh38
NC_000019.9:g.57746340A>G , CM000681.1:g.57746340A>G	GRCh37
NC_000019.8:g.62438152A>G	NCBI36
NG_012134.1:g.8964A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.673A>G MANE Select	ENSP00000302898.6:p.Ile225Val
ENST00000302804.11:c.673A>G	ENSP00000302898.6:p.Ile225Val
ENST00000415300.6:c.616A>G	ENSP00000407162.1:p.Ile206Val
ENST00000448930.5:c.568A>G	ENSP00000406798.2:p.Ile190Val
ENST00000594599.1:c.157A>G	ENSP00000469894.1:p.Ile53Val
ENST00000596375.1:c.*234A>G	ENSP00000470465.1:n.*234A>G
ENST00000598785.5:c.571A>G	ENSP00000471830.1:p.Ile191Val
ENST00000599062.5:c.664A>G	ENSP00000469983.1:p.Ile222Val
ENST00000601799.5:c.*972A>G	ENSP00000468918.1:n.*972A>G
NM_001015878.1:c.673A>G	NP_001015878.1:p.Ile225Val
NM_001015879.1:c.616A>G	NP_001015879.1:p.Ile206Val
NM_003160.2:c.571A>G	NP_003151.2:p.Ile191Val
XR_430209.2:n.1567A>G
XR_430209.3:n.1610A>G
NM_001015878.2:c.673A>G MANE Select	NP_001015878.1:p.Ile225Val
NM_001015879.2:c.616A>G	NP_001015879.1:p.Ile206Val
NM_003160.3:c.571A>G	NP_003151.2:p.Ile191Val