Canonical Allele Identifier: CA9695794

Gene: AURKC

Linked Data

• dbSNP Id: rs754876967
• ExAC: 19:57742483 G / A
• gnomAD v2: 19-57742483-G-A
• gnomAD v3: 19-57231115-G-A
• gnomAD v4: 19-57231115-G-A
• MyVariant Identifiers: chr19:g.57742483G>A (hg19) ; chr19:g.57231115G>A (hg38)

Genomic Alleles

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

Transcript Alleles

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