Canonical Allele Identifier: CA407692960

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746325G>C (hg19) ; chr19:g.57234957G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234957G>C , CM000681.2:g.57234957G>C	GRCh38
NC_000019.9:g.57746325G>C , CM000681.1:g.57746325G>C	GRCh37
NC_000019.8:g.62438137G>C	NCBI36
NG_012134.1:g.8949G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.658G>C MANE Select	ENSP00000302898.6:p.Val220Leu
ENST00000302804.11:c.658G>C	ENSP00000302898.6:p.Val220Leu
ENST00000415300.6:c.601G>C	ENSP00000407162.1:p.Val201Leu
ENST00000448930.5:c.553G>C	ENSP00000406798.2:p.Val185Leu
ENST00000594599.1:c.142G>C	ENSP00000469894.1:p.Val48Leu
ENST00000596375.1:c.*219G>C	ENSP00000470465.1:n.*219G>C
ENST00000598785.5:c.556G>C	ENSP00000471830.1:p.Val186Leu
ENST00000599062.5:c.649G>C	ENSP00000469983.1:p.Val217Leu
ENST00000601799.5:c.*957G>C	ENSP00000468918.1:n.*957G>C
NM_001015878.1:c.658G>C	NP_001015878.1:p.Val220Leu
NM_001015879.1:c.601G>C	NP_001015879.1:p.Val201Leu
NM_003160.2:c.556G>C	NP_003151.2:p.Val186Leu
XR_430209.2:n.1552G>C
XR_430209.3:n.1595G>C
NM_001015878.2:c.658G>C MANE Select	NP_001015878.1:p.Val220Leu
NM_001015879.2:c.601G>C	NP_001015879.1:p.Val201Leu
NM_003160.3:c.556G>C	NP_003151.2:p.Val186Leu