Canonical Allele Identifier: CA973886387
Gene: SLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3590272_3590275del , CM000678.2:g.3590272_3590275del GRCh38
NC_000016.9:g.3640273_3640276del , CM000678.1:g.3640273_3640276del GRCh37
NC_000016.8:g.3580274_3580277del NCBI36
NG_028123.1:g.26312_26315del , LRG_503:g.26312_26315del

Transcript Alleles

HGVS Amino-acid Change
NM_032444.4:c.3365_3368del MANE Select NP_115820.2:p.Pro1122LeufsTer4
ENST00000294008.4:c.3365_3368del MANE Select ENSP00000294008.3:p.Pro1122LeufsTer4
NM_032444.2:c.3365_3368del , LRG_503t1:c.3365_3368del NP_115820.2:p.Pro1122LeufsTer4
NM_032444.3:c.3365_3368del NP_115820.2:p.Pro1122LeufsTer4
ENST00000294008.3:c.3365_3368del ENSP00000294008.3:p.Pro1122LeufsTer4
XM_011522715.1:c.3365_3368del XP_011521017.1:p.Pro1122LeufsTer4
XM_011522715.3:c.3365_3368del XP_011521017.1:p.Pro1122LeufsTer4
XM_017023775.2:c.2543_2546del XP_016879264.1:p.Pro848LeufsTer4
XM_024450471.1:c.3365_3368del XP_024306239.1:p.Pro1122LeufsTer4