Canonical Allele Identifier: CA407692614

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746278A>T (hg19) ; chr19:g.57234910A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234910A>T , CM000681.2:g.57234910A>T	GRCh38
NC_000019.9:g.57746278A>T , CM000681.1:g.57746278A>T	GRCh37
NC_000019.8:g.62438090A>T	NCBI36
NG_012134.1:g.8902A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.611A>T MANE Select	ENSP00000302898.6:p.Asp204Val
ENST00000302804.11:c.611A>T	ENSP00000302898.6:p.Asp204Val
ENST00000415300.6:c.554A>T	ENSP00000407162.1:p.Asp185Val
ENST00000448930.5:c.506A>T	ENSP00000406798.2:p.Asp169Val
ENST00000594599.1:c.95A>T	ENSP00000469894.1:p.Asp32Val
ENST00000596375.1:c.*172A>T	ENSP00000470465.1:n.*172A>T
ENST00000598785.5:c.509A>T	ENSP00000471830.1:p.Asp170Val
ENST00000599062.5:c.602A>T	ENSP00000469983.1:p.Asp201Val
ENST00000601799.5:c.*910A>T	ENSP00000468918.1:n.*910A>T
NM_001015878.1:c.611A>T	NP_001015878.1:p.Asp204Val
NM_001015879.1:c.554A>T	NP_001015879.1:p.Asp185Val
NM_003160.2:c.509A>T	NP_003151.2:p.Asp170Val
XR_430209.2:n.1505A>T
XR_430209.3:n.1548A>T
NM_001015878.2:c.611A>T MANE Select	NP_001015878.1:p.Asp204Val
NM_001015879.2:c.554A>T	NP_001015879.1:p.Asp185Val
NM_003160.3:c.509A>T	NP_003151.2:p.Asp170Val