Canonical Allele Identifier: CA407693040

Gene: AURKC

Linked Data

• dbSNP Id: rs1429695197
• gnomAD v2: 19-57746341-T-C
• gnomAD v3: 19-57234973-T-C
• gnomAD v4: 19-57234973-T-C
• MyVariant Identifiers: chr19:g.57746341T>C (hg19) ; chr19:g.57234973T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234973T>C , CM000681.2:g.57234973T>C	GRCh38
NC_000019.9:g.57746341T>C , CM000681.1:g.57746341T>C	GRCh37
NC_000019.8:g.62438153T>C	NCBI36
NG_012134.1:g.8965T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.674T>C MANE Select	ENSP00000302898.6:p.Ile225Thr
ENST00000302804.11:c.674T>C	ENSP00000302898.6:p.Ile225Thr
ENST00000415300.6:c.617T>C	ENSP00000407162.1:p.Ile206Thr
ENST00000448930.5:c.569T>C	ENSP00000406798.2:p.Ile190Thr
ENST00000594599.1:c.158T>C	ENSP00000469894.1:p.Ile53Thr
ENST00000596375.1:c.*235T>C	ENSP00000470465.1:n.*235T>C
ENST00000598785.5:c.572T>C	ENSP00000471830.1:p.Ile191Thr
ENST00000599062.5:c.665T>C	ENSP00000469983.1:p.Ile222Thr
ENST00000601799.5:c.*973T>C	ENSP00000468918.1:n.*973T>C
NM_001015878.1:c.674T>C	NP_001015878.1:p.Ile225Thr
NM_001015879.1:c.617T>C	NP_001015879.1:p.Ile206Thr
NM_003160.2:c.572T>C	NP_003151.2:p.Ile191Thr
XR_430209.2:n.1568T>C
XR_430209.3:n.1611T>C
NM_001015878.2:c.674T>C MANE Select	NP_001015878.1:p.Ile225Thr
NM_001015879.2:c.617T>C	NP_001015879.1:p.Ile206Thr
NM_003160.3:c.572T>C	NP_003151.2:p.Ile191Thr