Canonical Allele Identifier: CA394520078
Gene: SLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3590172C>G , CM000678.2:g.3590172C>G GRCh38
NC_000016.9:g.3640173C>G , CM000678.1:g.3640173C>G GRCh37
NC_000016.8:g.3580174C>G NCBI36
NG_028123.1:g.26413G>C , LRG_503:g.26413G>C

Transcript Alleles

HGVS Amino-acid Change
NM_032444.4:c.3466G>C MANE Select NP_115820.2:p.Asp1156His
ENST00000294008.4:c.3466G>C MANE Select ENSP00000294008.3:p.Asp1156His
NM_032444.2:c.3466G>C , LRG_503t1:c.3466G>C NP_115820.2:p.Asp1156His
NM_032444.3:c.3466G>C NP_115820.2:p.Asp1156His
ENST00000294008.3:c.3466G>C ENSP00000294008.3:p.Asp1156His
XM_011522715.1:c.3466G>C XP_011521017.1:p.Asp1156His
XM_011522715.3:c.3466G>C XP_011521017.1:p.Asp1156His
XM_017023775.2:c.2644G>C XP_016879264.1:p.Asp882His
XM_024450471.1:c.3466G>C XP_024306239.1:p.Asp1156His