Canonical Allele Identifier: CA407692910

Gene: AURKC

Linked Data

• dbSNP Id: rs1380978382
• gnomAD v2: 19-57746316-G-T
• gnomAD v4: 19-57234948-G-T
• MyVariant Identifiers: chr19:g.57746316G>T (hg19) ; chr19:g.57234948G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234948G>T , CM000681.2:g.57234948G>T	GRCh38
NC_000019.9:g.57746316G>T , CM000681.1:g.57746316G>T	GRCh37
NC_000019.8:g.62438128G>T	NCBI36
NG_012134.1:g.8940G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.649G>T MANE Select	ENSP00000302898.6:p.Asp217Tyr
ENST00000302804.11:c.649G>T	ENSP00000302898.6:p.Asp217Tyr
ENST00000415300.6:c.592G>T	ENSP00000407162.1:p.Asp198Tyr
ENST00000448930.5:c.544G>T	ENSP00000406798.2:p.Asp182Tyr
ENST00000594599.1:c.133G>T	ENSP00000469894.1:p.Asp45Tyr
ENST00000596375.1:c.*210G>T	ENSP00000470465.1:n.*210G>T
ENST00000598785.5:c.547G>T	ENSP00000471830.1:p.Asp183Tyr
ENST00000599062.5:c.640G>T	ENSP00000469983.1:p.Asp214Tyr
ENST00000601799.5:c.*948G>T	ENSP00000468918.1:n.*948G>T
NM_001015878.1:c.649G>T	NP_001015878.1:p.Asp217Tyr
NM_001015879.1:c.592G>T	NP_001015879.1:p.Asp198Tyr
NM_003160.2:c.547G>T	NP_003151.2:p.Asp183Tyr
XR_430209.2:n.1543G>T
XR_430209.3:n.1586G>T
NM_001015878.2:c.649G>T MANE Select	NP_001015878.1:p.Asp217Tyr
NM_001015879.2:c.592G>T	NP_001015879.1:p.Asp198Tyr
NM_003160.3:c.547G>T	NP_003151.2:p.Asp183Tyr