Canonical Allele Identifier: CA407688573

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57742483G>T (hg19) ; chr19:g.57231115G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57231115G>T , CM000681.2:g.57231115G>T	GRCh38
NC_000019.9:g.57742483G>T , CM000681.1:g.57742483G>T	GRCh37
NC_000019.8:g.62434295G>T	NCBI36
NG_012134.1:g.5107G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.-134G>T MANE Select	ENSP00000302898.6:n.-134G>T
ENST00000302804.11:c.-134G>T	ENSP00000302898.6:n.-134G>T
ENST00000415300.6:c.1+1G>T	ENSP00000407162.1:n.1+1G>T
ENST00000448930.5:c.-50G>T	ENSP00000406798.2:n.-50G>T
NM_001015878.1:c.-134G>T	NP_001015878.1:n.-134G>T
NM_001015879.1:c.1+1G>T	NP_001015879.1:n.1+1G>T
NM_003160.2:c.-49G>T	NP_003151.2:n.-49G>T
XR_430209.2:n.756G>T
XR_430209.3:n.799G>T
NM_001015878.2:c.-134G>T MANE Select	NP_001015878.1:n.-134G>T
NM_001015879.2:c.1+1G>T	NP_001015879.1:n.1+1G>T
NM_003160.3:c.-49G>T	NP_003151.2:n.-49G>T