Canonical Allele Identifier: CA7866150
Gene: SLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3591201C>T , CM000678.2:g.3591201C>T GRCh38
NC_000016.9:g.3641202C>T , CM000678.1:g.3641202C>T GRCh37
NC_000016.8:g.3581203C>T NCBI36
NG_028123.1:g.25384G>A , LRG_503:g.25384G>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000294008.4:c.2437G>A MANE Select ENSP00000294008.3:p.Glu813Lys
ENST00000294008.3:c.2437G>A ENSP00000294008.3:p.Glu813Lys
NM_032444.2:c.2437G>A , LRG_503t1:c.2437G>A NP_115820.2:p.Glu813Lys
XM_011522715.1:c.2437G>A XP_011521017.1:p.Glu813Lys
NM_032444.3:c.2437G>A NP_115820.2:p.Glu813Lys
XM_011522715.3:c.2437G>A XP_011521017.1:p.Glu813Lys
XM_017023775.2:c.1615G>A XP_016879264.1:p.Glu539Lys
XM_024450471.1:c.2437G>A XP_024306239.1:p.Glu813Lys
NM_032444.4:c.2437G>A MANE Select NP_115820.2:p.Glu813Lys