Canonical Allele Identifier: CA358898

Gene: SLFN14

Linked Data

• ClinVar Variation Id: 225535
• ClinVar RCV Id: RCV000210920 ; RCV001267345
• dbSNP Id: rs869320716
• MyVariant Identifiers: chr17:g.33884430T>C (hg19) ; chr17:g.35557411T>C (hg38)
• PubMed: PMID:26280575

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35557411T>C , CM000679.2:g.35557411T>C	GRCh38
NC_000017.10:g.33884430T>C , CM000679.1:g.33884430T>C	GRCh37
NC_000017.9:g.30908543T>C	NCBI36
NG_051181.1:g.8431A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000674182.1:c.652A>G MANE Select	ENSP00000501524.1:p.Lys218Glu
ENST00000415846.3:c.652A>G	ENSP00000391101.2:p.Lys218Glu
NM_001129820.1:c.652A>G	NP_001123292.1:p.Lys218Glu
XM_005257968.2:c.652A>G	XP_005258025.2:p.Lys218Glu
XM_011524741.1:c.652A>G	XP_011523043.1:p.Lys218Glu
XM_011524742.1:c.652A>G	XP_011523044.1:p.Lys218Glu
XM_011524743.1:c.652A>G	XP_011523045.1:p.Lys218Glu
XM_017024576.1:c.652A>G	XP_016880065.1:p.Lys218Glu
XM_017024577.1:c.652A>G	XP_016880066.1:p.Lys218Glu
XM_017024578.1:c.652A>G	XP_016880067.1:p.Lys218Glu
XM_017024579.1:c.652A>G	XP_016880068.1:p.Lys218Glu
NM_001129820.2:c.652A>G MANE Select	NP_001123292.1:p.Lys218Glu