Canonical Allele Identifier: CA509133426

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746331T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234963T>C , CM000681.2:g.57234963T>C	GRCh38
NC_000019.9:g.57746331T>C , CM000681.1:g.57746331T>C	GRCh37
NC_000019.8:g.62438143T>C	NCBI36
NG_012134.1:g.8955T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.664T>C MANE Select	ENSP00000302898.6:p.Leu222=
ENST00000302804.11:c.664T>C	ENSP00000302898.6:p.Leu222=
ENST00000415300.6:c.607T>C	ENSP00000407162.1:p.Leu203=
ENST00000448930.5:c.559T>C	ENSP00000406798.2:p.Leu187=
ENST00000594599.1:c.148T>C	ENSP00000469894.1:p.Leu50=
ENST00000596375.1:c.*225T>C	ENSP00000470465.1:n.*225T>C
ENST00000598785.5:c.562T>C	ENSP00000471830.1:p.Leu188=
ENST00000599062.5:c.655T>C	ENSP00000469983.1:p.Leu219=
ENST00000601799.5:c.*963T>C	ENSP00000468918.1:n.*963T>C
NM_001015878.1:c.664T>C	NP_001015878.1:p.Leu222=
NM_001015879.1:c.607T>C	NP_001015879.1:p.Leu203=
NM_003160.2:c.562T>C	NP_003151.2:p.Leu188=
XR_430209.2:n.1558T>C
XR_430209.3:n.1601T>C
NM_001015878.2:c.664T>C MANE Select	NP_001015878.1:p.Leu222=
NM_001015879.2:c.607T>C	NP_001015879.1:p.Leu203=
NM_003160.3:c.562T>C	NP_003151.2:p.Leu188=