Canonical Allele Identifier: CA7866769

Gene: SLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3606481C>T , CM000678.2:g.3606481C>T	GRCh38
NC_000016.9:g.3656482C>T , CM000678.1:g.3656482C>T	GRCh37
NC_000016.8:g.3596483C>T	NCBI36
NG_028123.1:g.10104G>A , LRG_503:g.10104G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697858.1:n.94G>A
ENST00000294008.4:c.753G>A MANE Select	ENSP00000294008.3:p.Ala251=
ENST00000294008.3:c.753G>A	ENSP00000294008.3:p.Ala251=
ENST00000466154.5:n.1048G>A
ENST00000486524.1:n.1381G>A
NM_032444.2:c.753G>A , LRG_503t1:c.753G>A	NP_115820.2:p.Ala251=
XM_011522715.1:c.753G>A	XP_011521017.1:p.Ala251=
NM_032444.3:c.753G>A	NP_115820.2:p.Ala251=
XM_011522715.3:c.753G>A	XP_011521017.1:p.Ala251=
XM_024450471.1:c.753G>A	XP_024306239.1:p.Ala251=
NM_032444.4:c.753G>A MANE Select	NP_115820.2:p.Ala251=