Canonical Allele Identifier: CA407693065

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746347T>A (hg19) ; chr19:g.57234979T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234979T>A , CM000681.2:g.57234979T>A	GRCh38
NC_000019.9:g.57746347T>A , CM000681.1:g.57746347T>A	GRCh37
NC_000019.8:g.62438159T>A	NCBI36
NG_012134.1:g.8971T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.680T>A MANE Select	ENSP00000302898.6:p.Val227Glu
ENST00000302804.11:c.680T>A	ENSP00000302898.6:p.Val227Glu
ENST00000415300.6:c.623T>A	ENSP00000407162.1:p.Val208Glu
ENST00000448930.5:c.575T>A	ENSP00000406798.2:p.Val192Glu
ENST00000594599.1:c.164T>A	ENSP00000469894.1:p.Val55Glu
ENST00000596375.1:c.*241T>A	ENSP00000470465.1:n.*241T>A
ENST00000598785.5:c.578T>A	ENSP00000471830.1:p.Val193Glu
ENST00000599062.5:c.671T>A	ENSP00000469983.1:p.Val224Glu
ENST00000601799.5:c.*979T>A	ENSP00000468918.1:n.*979T>A
NM_001015878.1:c.680T>A	NP_001015878.1:p.Val227Glu
NM_001015879.1:c.623T>A	NP_001015879.1:p.Val208Glu
NM_003160.2:c.578T>A	NP_003151.2:p.Val193Glu
XR_430209.2:n.1574T>A
XR_430209.3:n.1617T>A
NM_001015878.2:c.680T>A MANE Select	NP_001015878.1:p.Val227Glu
NM_001015879.2:c.623T>A	NP_001015879.1:p.Val208Glu
NM_003160.3:c.578T>A	NP_003151.2:p.Val193Glu