Canonical Allele Identifier: CA407692678

Gene: AURKC

Linked Data

• MyVariant Identifiers: chr19:g.57746284T>G (hg19) ; chr19:g.57234916T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57234916T>G , CM000681.2:g.57234916T>G	GRCh38
NC_000019.9:g.57746284T>G , CM000681.1:g.57746284T>G	GRCh37
NC_000019.8:g.62438096T>G	NCBI36
NG_012134.1:g.8908T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302804.12:c.617T>G MANE Select	ENSP00000302898.6:p.Leu206Trp
ENST00000302804.11:c.617T>G	ENSP00000302898.6:p.Leu206Trp
ENST00000415300.6:c.560T>G	ENSP00000407162.1:p.Leu187Trp
ENST00000448930.5:c.512T>G	ENSP00000406798.2:p.Leu171Trp
ENST00000594599.1:c.101T>G	ENSP00000469894.1:p.Leu34Trp
ENST00000596375.1:c.*178T>G	ENSP00000470465.1:n.*178T>G
ENST00000598785.5:c.515T>G	ENSP00000471830.1:p.Leu172Trp
ENST00000599062.5:c.608T>G	ENSP00000469983.1:p.Leu203Trp
ENST00000601799.5:c.*916T>G	ENSP00000468918.1:n.*916T>G
NM_001015878.1:c.617T>G	NP_001015878.1:p.Leu206Trp
NM_001015879.1:c.560T>G	NP_001015879.1:p.Leu187Trp
NM_003160.2:c.515T>G	NP_003151.2:p.Leu172Trp
XR_430209.2:n.1511T>G
XR_430209.3:n.1554T>G
NM_001015878.2:c.617T>G MANE Select	NP_001015878.1:p.Leu206Trp
NM_001015879.2:c.560T>G	NP_001015879.1:p.Leu187Trp
NM_003160.3:c.515T>G	NP_003151.2:p.Leu172Trp