Canonical Allele Identifier: CA2257508435

Gene: SLFN13

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.35445639G= , CM000679.2:g.35445639G=	GRCh38
NC_000017.10:g.33772658G= , CM000679.1:g.33772658G=	GRCh37
NC_000017.9:g.30796771G=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_144682.6:c.42C= MANE Select	NP_653283.3:p.Tyr14=
ENST00000285013.11:c.42C= MANE Select	ENSP00000285013.6:p.Tyr14=
NM_144682.5:c.42C=	NP_653283.3:p.Tyr14=
ENST00000285013.10:c.42C=	ENSP00000285013.6:p.Tyr14=
ENST00000524511.5:c.42C=	ENSP00000433181.1:p.Tyr14=
ENST00000526861.5:c.42C=	ENSP00000434439.1:p.Tyr14=
ENST00000530782.5:c.42C=	ENSP00000437298.1:p.Tyr14=
ENST00000531588.1:c.42C=	ENSP00000467557.1:p.Tyr14=
ENST00000532210.5:c.-14-938C=	ENSP00000435328.1:n.-14-938C=
ENST00000533791.5:c.42C=	ENSP00000467426.1:p.Tyr14=
ENST00000534689.5:c.25+17C=	ENSP00000435442.1:n.25+17C=
ENST00000542635.5:c.42C=	ENSP00000444016.1:p.Tyr14=
XM_005257922.1:c.42C=	XP_005257979.1:p.Tyr14=
XM_005257922.2:c.42C=	XP_005257979.1:p.Tyr14=
XM_005257923.1:c.42C=	XP_005257980.1:p.Tyr14=
XM_011524382.1:c.42C=	XP_011522684.1:p.Tyr14=
XM_011524383.1:c.-14-938C=	XP_011522685.1:n.-14-938C=
XM_011524383.2:c.-14-938C=	XP_011522685.1:n.-14-938C=
XM_017024232.1:c.42C=	XP_016879721.1:p.Tyr14=
XM_017024233.1:c.42C=	XP_016879722.1:p.Tyr14=
XM_024450614.1:c.42C=	XP_024306382.1:p.Tyr14=
XM_024450615.1:c.42C=	XP_024306383.1:p.Tyr14=
XM_024450616.1:c.42C=	XP_024306384.1:p.Tyr14=