Canonical Allele Identifier: CA407693035

Gene: AURKC

Linked Data

• dbSNP Id: rs2087531769
• MyVariant Identifiers: chr19:g.57746340A>C (hg19) ; chr19:g.57234972A>C (hg38)

Genomic Alleles

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

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.673A>C MANE Select	ENSP00000302898.6:p.Ile225Leu
ENST00000302804.11:c.673A>C	ENSP00000302898.6:p.Ile225Leu
ENST00000415300.6:c.616A>C	ENSP00000407162.1:p.Ile206Leu
ENST00000448930.5:c.568A>C	ENSP00000406798.2:p.Ile190Leu
ENST00000594599.1:c.157A>C	ENSP00000469894.1:p.Ile53Leu
ENST00000596375.1:c.*234A>C	ENSP00000470465.1:n.*234A>C
ENST00000598785.5:c.571A>C	ENSP00000471830.1:p.Ile191Leu
ENST00000599062.5:c.664A>C	ENSP00000469983.1:p.Ile222Leu
ENST00000601799.5:c.*972A>C	ENSP00000468918.1:n.*972A>C
NM_001015878.1:c.673A>C	NP_001015878.1:p.Ile225Leu
NM_001015879.1:c.616A>C	NP_001015879.1:p.Ile206Leu
NM_003160.2:c.571A>C	NP_003151.2:p.Ile191Leu
XR_430209.2:n.1567A>C
XR_430209.3:n.1610A>C
NM_001015878.2:c.673A>C MANE Select	NP_001015878.1:p.Ile225Leu
NM_001015879.2:c.616A>C	NP_001015879.1:p.Ile206Leu
NM_003160.3:c.571A>C	NP_003151.2:p.Ile191Leu