Canonical Allele Identifier: CA407692532

Gene: AURKC

Linked Data

• gnomAD v4: 19-57234896-G-A
• MyVariant Identifiers: chr19:g.57746264G>A (hg19) ; chr19:g.57234896G>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234896G>A , CM000681.2:g.57234896G>A	GRCh38
NC_000019.9:g.57746264G>A , CM000681.1:g.57746264G>A	GRCh37
NC_000019.8:g.62438076G>A	NCBI36
NG_012134.1:g.8888G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.597G>A MANE Select	ENSP00000302898.6:p.Met199Ile
ENST00000302804.11:c.597G>A	ENSP00000302898.6:p.Met199Ile
ENST00000415300.6:c.540G>A	ENSP00000407162.1:p.Met180Ile
ENST00000448930.5:c.492G>A	ENSP00000406798.2:p.Met164Ile
ENST00000594599.1:c.81G>A	ENSP00000469894.1:p.Met27Ile
ENST00000596375.1:c.*158G>A	ENSP00000470465.1:n.*158G>A
ENST00000598785.5:c.495G>A	ENSP00000471830.1:p.Met165Ile
ENST00000599062.5:c.588G>A	ENSP00000469983.1:p.Met196Ile
ENST00000601799.5:c.*896G>A	ENSP00000468918.1:n.*896G>A
NM_001015878.1:c.597G>A	NP_001015878.1:p.Met199Ile
NM_001015879.1:c.540G>A	NP_001015879.1:p.Met180Ile
NM_003160.2:c.495G>A	NP_003151.2:p.Met165Ile
XR_430209.2:n.1491G>A
XR_430209.3:n.1534G>A
NM_001015878.2:c.597G>A MANE Select	NP_001015878.1:p.Met199Ile
NM_001015879.2:c.540G>A	NP_001015879.1:p.Met180Ile
NM_003160.3:c.495G>A	NP_003151.2:p.Met165Ile