Canonical Allele Identifier: CA8504564
Gene: SLFN14 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.35548829del , CM000679.2:g.35548829del GRCh38
NC_000017.10:g.33875848del , CM000679.1:g.33875848del GRCh37
NC_000017.9:g.30899961del NCBI36
NG_051181.1:g.17017del

Transcript Alleles

HGVS Amino-acid Change
NM_001129820.2:c.2153del MANE Select NP_001123292.1:p.Pro718LeufsTer21
ENST00000674182.1:c.2153del MANE Select ENSP00000501524.1:p.Pro718LeufsTer21
NM_001129820.1:c.2153del NP_001123292.1:p.Pro718LeufsTer21
ENST00000415846.3:c.2153del ENSP00000391101.2:p.Pro718LeufsTer21
XM_005257968.2:c.2201del XP_005258025.2:p.Pro734LeufsTer21
XM_011524741.1:c.2201del XP_011523043.1:p.Pro734LeufsTer21
XM_011524742.1:c.2201del XP_011523044.1:p.Pro734LeufsTer21
XM_011524743.1:c.2153del XP_011523045.1:p.Pro718LeufsTer21
XM_017024576.1:c.2153del XP_016880065.1:p.Pro718LeufsTer21
XM_017024577.1:c.2153del XP_016880066.1:p.Pro718LeufsTer21
XM_017024578.1:c.2153del XP_016880067.1:p.Pro718LeufsTer21
XM_017024579.1:c.2153del XP_016880068.1:p.Pro718LeufsTer21
XR_001752849.1:n.520-3175del