Canonical Allele Identifier: CA407692786

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746297G>C (hg19) ; chr19:g.57234929G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234929G>C , CM000681.2:g.57234929G>C	GRCh38
NC_000019.9:g.57746297G>C , CM000681.1:g.57746297G>C	GRCh37
NC_000019.8:g.62438109G>C	NCBI36
NG_012134.1:g.8921G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.630G>C MANE Select	ENSP00000302898.6:p.Met210Ile
ENST00000302804.11:c.630G>C	ENSP00000302898.6:p.Met210Ile
ENST00000415300.6:c.573G>C	ENSP00000407162.1:p.Met191Ile
ENST00000448930.5:c.525G>C	ENSP00000406798.2:p.Met175Ile
ENST00000594599.1:c.114G>C	ENSP00000469894.1:p.Met38Ile
ENST00000596375.1:c.*191G>C	ENSP00000470465.1:n.*191G>C
ENST00000598785.5:c.528G>C	ENSP00000471830.1:p.Met176Ile
ENST00000599062.5:c.621G>C	ENSP00000469983.1:p.Met207Ile
ENST00000601799.5:c.*929G>C	ENSP00000468918.1:n.*929G>C
NM_001015878.1:c.630G>C	NP_001015878.1:p.Met210Ile
NM_001015879.1:c.573G>C	NP_001015879.1:p.Met191Ile
NM_003160.2:c.528G>C	NP_003151.2:p.Met176Ile
XR_430209.2:n.1524G>C
XR_430209.3:n.1567G>C
NM_001015878.2:c.630G>C MANE Select	NP_001015878.1:p.Met210Ile
NM_001015879.2:c.573G>C	NP_001015879.1:p.Met191Ile
NM_003160.3:c.528G>C	NP_003151.2:p.Met176Ile