Canonical Allele Identifier: CA7865421

Gene: SLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3583104A>T , CM000678.2:g.3583104A>T	GRCh38
NC_000016.9:g.3633105A>T , CM000678.1:g.3633105A>T	GRCh37
NC_000016.8:g.3573106A>T	NCBI36
NG_028123.1:g.33481T>A , LRG_503:g.33481T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294008.4:c.5146T>A MANE Select	ENSP00000294008.3:p.Ser1716Thr
ENST00000294008.3:c.5146T>A	ENSP00000294008.3:p.Ser1716Thr
NM_032444.2:c.5146T>A , LRG_503t1:c.5146T>A	NP_115820.2:p.Ser1716Thr
XM_011522715.1:c.5143T>A	XP_011521017.1:p.Ser1715Thr
NM_032444.3:c.5146T>A	NP_115820.2:p.Ser1716Thr
XM_011522715.3:c.5143T>A	XP_011521017.1:p.Ser1715Thr
XM_017023775.2:c.4324T>A	XP_016879264.1:p.Ser1442Thr
XM_024450471.1:c.5146T>A	XP_024306239.1:p.Ser1716Thr
NM_032444.4:c.5146T>A MANE Select	NP_115820.2:p.Ser1716Thr