Canonical Allele Identifier: CA339909955

Gene: SLFNL1 SLFNL1-AS1

Linked Data

• ClinVar Variation Id: 2608139
• ClinVar RCV Id: RCV004357264
• MyVariant Identifiers: chr1:g.41486073C>T (hg19) ; chr1:g.41020401C>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.41020401C>T , CM000663.2:g.41020401C>T	GRCh38
NC_000001.10:g.41486073C>T , CM000663.1:g.41486073C>T	GRCh37
NC_000001.9:g.41258660C>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302946.13:c.260G>A (SLFNL1) MANE Select	ENSP00000304401.8:p.Arg87Lys
ENST00000688905.1:n.463G>A (SLFNL1)
ENST00000693284.1:c.260G>A (SLFNL1)	ENSP00000509946.1:p.Arg87Lys
ENST00000302946.12:c.260G>A (SLFNL1)	ENSP00000304401.8:p.Arg87Lys
ENST00000359345.5:c.260G>A (SLFNL1)	ENSP00000352299.1:p.Arg87Lys
ENST00000372611.5:c.260G>A (SLFNL1)	ENSP00000361694.1:p.Arg87Lys
ENST00000372613.6:c.260G>A (SLFNL1)	ENSP00000361696.2:p.Arg87Lys
ENST00000439569.2:c.260G>A (SLFNL1)	ENSP00000398938.2:p.Arg87Lys
NM_001168247.2:c.260G>A (SLFNL1)	NP_001161719.1:p.Arg87Lys
NM_001300859.1:c.260G>A (SLFNL1)	NP_001287788.1:p.Arg87Lys
NM_144990.3:c.260G>A (SLFNL1)	NP_659427.3:p.Arg87Lys
NR_037868.1:n.3812+2000C>T (SLFNL1-AS1)
XM_005270596.2:c.260G>A (SLFNL1)	XP_005270653.1:p.Arg87Lys
XM_005270597.2:c.260G>A (SLFNL1)	XP_005270654.1:p.Arg87Lys
XM_005270598.2:c.260G>A (SLFNL1)	XP_005270655.1:p.Arg87Lys
XM_005270599.2:c.260G>A (SLFNL1)	XP_005270656.1:p.Arg87Lys
XM_005270600.2:c.260G>A (SLFNL1)	XP_005270657.1:p.Arg87Lys
XM_005270601.2:c.260G>A (SLFNL1)	XP_005270658.1:p.Arg87Lys
XM_006710432.2:c.260G>A (SLFNL1)	XP_006710495.1:p.Arg87Lys
XM_011540943.1:c.260G>A (SLFNL1)	XP_011539245.1:p.Arg87Lys
XM_011540944.1:c.260G>A (SLFNL1)	XP_011539246.1:p.Arg87Lys
XM_011540945.1:c.260G>A (SLFNL1)	XP_011539247.1:p.Arg87Lys
XM_011540946.1:c.260G>A (SLFNL1)	XP_011539248.1:p.Arg87Lys
XM_011540947.1:c.260G>A (SLFNL1)	XP_011539249.1:p.Arg87Lys
XM_011540948.1:c.260G>A (SLFNL1)	XP_011539250.1:p.Arg87Lys
XM_011540949.1:c.260G>A (SLFNL1)	XP_011539251.1:p.Arg87Lys
XM_011540950.1:c.260G>A (SLFNL1)	XP_011539252.1:p.Arg87Lys
XM_011540951.1:c.260G>A (SLFNL1)	XP_011539253.1:p.Arg87Lys
XM_011540952.1:c.260G>A (SLFNL1)	XP_011539254.1:p.Arg87Lys
XM_011540953.1:c.260G>A (SLFNL1)	XP_011539255.1:p.Arg87Lys
XM_011540954.1:c.260G>A (SLFNL1)	XP_011539256.1:p.Arg87Lys
XM_011540955.1:c.260G>A (SLFNL1)	XP_011539257.1:p.Arg87Lys
XM_006710432.4:c.260G>A (SLFNL1)	XP_006710495.1:p.Arg87Lys
XM_011540945.2:c.260G>A (SLFNL1)	XP_011539247.1:p.Arg87Lys
XM_011540948.2:c.260G>A (SLFNL1)	XP_011539250.1:p.Arg87Lys
XM_011540949.2:c.260G>A (SLFNL1)	XP_011539251.1:p.Arg87Lys
XM_011540952.2:c.260G>A (SLFNL1)	XP_011539254.1:p.Arg87Lys
XM_011540953.3:c.260G>A (SLFNL1)	XP_011539255.1:p.Arg87Lys
XM_024453868.1:c.260G>A (SLFNL1)	XP_024309636.1:p.Arg87Lys
XM_024453869.1:c.260G>A (SLFNL1)	XP_024309637.1:p.Arg87Lys
NM_001300859.2:c.260G>A (SLFNL1)	NP_001287788.1:p.Arg87Lys
NM_144990.4:c.260G>A (SLFNL1) MANE Select	NP_659427.3:p.Arg87Lys
NM_001168247.3:c.260G>A (SLFNL1)	NP_001161719.1:p.Arg87Lys
NM_001377532.1:c.260G>A (SLFNL1)	NP_001364461.1:p.Arg87Lys
NM_001394331.1:c.260G>A (SLFNL1)	NP_001381260.1:p.Arg87Lys