Canonical Allele Identifier: CA7866061

Gene: SLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3590814C>G , CM000678.2:g.3590814C>G	GRCh38
NC_000016.9:g.3640815C>G , CM000678.1:g.3640815C>G	GRCh37
NC_000016.8:g.3580816C>G	NCBI36
NG_028123.1:g.25771G>C , LRG_503:g.25771G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294008.4:c.2824G>C MANE Select	ENSP00000294008.3:p.Glu942Gln
ENST00000294008.3:c.2824G>C	ENSP00000294008.3:p.Glu942Gln
NM_032444.2:c.2824G>C , LRG_503t1:c.2824G>C	NP_115820.2:p.Glu942Gln
XM_011522715.1:c.2824G>C	XP_011521017.1:p.Glu942Gln
NM_032444.3:c.2824G>C	NP_115820.2:p.Glu942Gln
XM_011522715.3:c.2824G>C	XP_011521017.1:p.Glu942Gln
XM_017023775.2:c.2002G>C	XP_016879264.1:p.Glu668Gln
XM_024450471.1:c.2824G>C	XP_024306239.1:p.Glu942Gln
NM_032444.4:c.2824G>C MANE Select	NP_115820.2:p.Glu942Gln