Canonical Allele Identifier: CA2257561715

Gene: SLFN14

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35557785T= , CM000679.2:g.35557785T=	GRCh38
NC_000017.10:g.33884804T= , CM000679.1:g.33884804T=	GRCh37
NC_000017.9:g.30908917T=	NCBI36
NG_051181.1:g.8057A=

Transcript Alleles

HGVS	Amino-acid Change
NM_001129820.2:c.278A= MANE Select	NP_001123292.1:p.Gln93=
ENST00000674182.1:c.278A= MANE Select	ENSP00000501524.1:p.Gln93=
NM_001129820.1:c.278A=	NP_001123292.1:p.Gln93=
ENST00000415846.3:c.278A=	ENSP00000391101.2:p.Gln93=
XM_005257968.2:c.278A=	XP_005258025.2:p.Gln93=
XM_011524741.1:c.278A=	XP_011523043.1:p.Gln93=
XM_011524742.1:c.278A=	XP_011523044.1:p.Gln93=
XM_011524743.1:c.278A=	XP_011523045.1:p.Gln93=
XM_017024576.1:c.278A=	XP_016880065.1:p.Gln93=
XM_017024577.1:c.278A=	XP_016880066.1:p.Gln93=
XM_017024578.1:c.278A=	XP_016880067.1:p.Gln93=
XM_017024579.1:c.278A=	XP_016880068.1:p.Gln93=