Canonical Allele Identifier: CA407688574

Gene: AURKC

Linked Data

• gnomAD v4: 19-57231116-T-A
• MyVariant Identifiers: chr19:g.57742484T>A (hg19) ; chr19:g.57231116T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57231116T>A , CM000681.2:g.57231116T>A	GRCh38
NC_000019.9:g.57742484T>A , CM000681.1:g.57742484T>A	GRCh37
NC_000019.8:g.62434296T>A	NCBI36
NG_012134.1:g.5108T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.-133T>A MANE Select	ENSP00000302898.6:n.-133T>A
ENST00000302804.11:c.-133T>A	ENSP00000302898.6:n.-133T>A
ENST00000415300.6:c.1+2T>A	ENSP00000407162.1:n.1+2T>A
ENST00000448930.5:c.-49T>A	ENSP00000406798.2:n.-49T>A
NM_001015878.1:c.-133T>A	NP_001015878.1:n.-133T>A
NM_001015879.1:c.1+2T>A	NP_001015879.1:n.1+2T>A
NM_003160.2:c.-48T>A	NP_003151.2:n.-48T>A
XR_430209.2:n.757T>A
XR_430209.3:n.800T>A
NM_001015878.2:c.-133T>A MANE Select	NP_001015878.1:n.-133T>A
NM_001015879.2:c.1+2T>A	NP_001015879.1:n.1+2T>A
NM_003160.3:c.-48T>A	NP_003151.2:n.-48T>A