Canonical Allele Identifier: CA2631404543
Gene: SLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3590184_3590186del , CM000678.2:g.3590184_3590186del GRCh38
NC_000016.9:g.3640185_3640187del , CM000678.1:g.3640185_3640187del GRCh37
NC_000016.8:g.3580186_3580188del NCBI36
NG_028123.1:g.26401_26403del , LRG_503:g.26401_26403del

Transcript Alleles

HGVS Amino-acid Change
NM_032444.4:c.3454_3456del MANE Select NP_115820.2:p.Ile1152del
ENST00000294008.4:c.3454_3456del MANE Select ENSP00000294008.3:p.Ile1152del
NM_032444.2:c.3454_3456del , LRG_503t1:c.3454_3456del NP_115820.2:p.Ile1152del
NM_032444.3:c.3454_3456del NP_115820.2:p.Ile1152del
ENST00000294008.3:c.3454_3456del ENSP00000294008.3:p.Ile1152del
XM_011522715.1:c.3454_3456del XP_011521017.1:p.Ile1152del
XM_011522715.3:c.3454_3456del XP_011521017.1:p.Ile1152del
XM_017023775.2:c.2632_2634del XP_016879264.1:p.Ile878del
XM_024450471.1:c.3454_3456del XP_024306239.1:p.Ile1152del