Canonical Allele Identifier: CA7866878

Gene: SLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3608542C>T , CM000678.2:g.3608542C>T	GRCh38
NC_000016.9:g.3658543C>T , CM000678.1:g.3658543C>T	GRCh37
NC_000016.8:g.3598544C>T	NCBI36
NG_028123.1:g.8043G>A , LRG_503:g.8043G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_032444.4:c.423G>A MANE Select	NP_115820.2:p.Gly141=
ENST00000294008.4:c.423G>A MANE Select	ENSP00000294008.3:p.Gly141=
NM_032444.2:c.423G>A , LRG_503t1:c.423G>A	NP_115820.2:p.Gly141=
NM_032444.3:c.423G>A	NP_115820.2:p.Gly141=
ENST00000294008.3:c.423G>A	ENSP00000294008.3:p.Gly141=
ENST00000466154.5:n.718G>A
ENST00000486524.1:n.1051G>A
ENST00000697859.1:n.1045G>A
XM_011522715.1:c.423G>A	XP_011521017.1:p.Gly141=
XM_011522715.3:c.423G>A	XP_011521017.1:p.Gly141=
XM_024450471.1:c.423G>A	XP_024306239.1:p.Gly141=