Canonical Allele Identifier: CA973886404
Gene: SLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3590274_3590275insCGACCACCG , CM000678.2:g.3590274_3590275insCGACCACCG GRCh38
NC_000016.9:g.3640275_3640276insCGACCACCG , CM000678.1:g.3640275_3640276insCGACCACCG GRCh37
NC_000016.8:g.3580276_3580277insCGACCACCG NCBI36
NG_028123.1:g.26311_26312insGGTGGTCGC , LRG_503:g.26311_26312insGGTGGTCGC

Transcript Alleles

HGVS Amino-acid Change
NM_032444.4:c.3364_3365insGGTGGTCGC MANE Select NP_115820.2:p.Ser1121_Pro1122insArgTrpSer
ENST00000294008.4:c.3364_3365insGGTGGTCGC MANE Select ENSP00000294008.3:p.Ser1121_Pro1122insArgTrpSer
NM_032444.2:c.3364_3365insGGTGGTCGC , LRG_503t1:c.3364_3365insGGTGGTCGC NP_115820.2:p.Ser1121_Pro1122insArgTrpSer
NM_032444.3:c.3364_3365insGGTGGTCGC NP_115820.2:p.Ser1121_Pro1122insArgTrpSer
ENST00000294008.3:c.3364_3365insGGTGGTCGC ENSP00000294008.3:p.Ser1121_Pro1122insArgTrpSer
XM_011522715.1:c.3364_3365insGGTGGTCGC XP_011521017.1:p.Ser1121_Pro1122insArgTrpSer
XM_011522715.3:c.3364_3365insGGTGGTCGC XP_011521017.1:p.Ser1121_Pro1122insArgTrpSer
XM_017023775.2:c.2542_2543insGGTGGTCGC XP_016879264.1:p.Ser847_Pro848insArgTrpSer
XM_024450471.1:c.3364_3365insGGTGGTCGC XP_024306239.1:p.Ser1121_Pro1122insArgTrpSer