Canonical Allele Identifier: CA310421675

Gene: AURKC

Linked Data

• dbSNP Id: rs999410039
• gnomAD v4: 19-57231027-G-T
• MyVariant Identifiers: chr19:g.57231027G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.57231027G>T , CM000681.2:g.57231027G>T	GRCh38
NC_000019.9:g.57742395G>T , CM000681.1:g.57742395G>T	GRCh37
NC_000019.8:g.62434207G>T	NCBI36
NG_012134.1:g.5019G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000302804.12:c.-222G>T MANE Select	ENSP00000302898.6:n.-222G>T
ENST00000415300.6:c.-87G>T	ENSP00000407162.1:n.-87G>T
ENST00000448930.5:c.-138G>T	ENSP00000406798.2:n.-138G>T
NM_001015879.1:c.-87G>T	NP_001015879.1:n.-87G>T
NM_003160.2:c.-137G>T	NP_003151.2:n.-137G>T
XR_430209.2:n.668G>T
XR_430209.3:n.711G>T
NM_001015878.2:c.-222G>T MANE Select	NP_001015878.1:n.-222G>T
NM_001015879.2:c.-87G>T	NP_001015879.1:n.-87G>T
NM_003160.3:c.-137G>T	NP_003151.2:n.-137G>T