Canonical Allele Identifier: CA407692906

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746315T>A (hg19) ; chr19:g.57234947T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234947T>A , CM000681.2:g.57234947T>A	GRCh38
NC_000019.9:g.57746315T>A , CM000681.1:g.57746315T>A	GRCh37
NC_000019.8:g.62438127T>A	NCBI36
NG_012134.1:g.8939T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.648T>A MANE Select	ENSP00000302898.6:p.Tyr216Ter
ENST00000302804.11:c.648T>A	ENSP00000302898.6:p.Tyr216Ter
ENST00000415300.6:c.591T>A	ENSP00000407162.1:p.Tyr197Ter
ENST00000448930.5:c.543T>A	ENSP00000406798.2:p.Tyr181Ter
ENST00000594599.1:c.132T>A	ENSP00000469894.1:p.Tyr44Ter
ENST00000596375.1:c.*209T>A	ENSP00000470465.1:n.*209T>A
ENST00000598785.5:c.546T>A	ENSP00000471830.1:p.Tyr182Ter
ENST00000599062.5:c.639T>A	ENSP00000469983.1:p.Tyr213Ter
ENST00000601799.5:c.*947T>A	ENSP00000468918.1:n.*947T>A
NM_001015878.1:c.648T>A	NP_001015878.1:p.Tyr216Ter
NM_001015879.1:c.591T>A	NP_001015879.1:p.Tyr197Ter
NM_003160.2:c.546T>A	NP_003151.2:p.Tyr182Ter
XR_430209.2:n.1542T>A
XR_430209.3:n.1585T>A
NM_001015878.2:c.648T>A MANE Select	NP_001015878.1:p.Tyr216Ter
NM_001015879.2:c.591T>A	NP_001015879.1:p.Tyr197Ter
NM_003160.3:c.546T>A	NP_003151.2:p.Tyr182Ter