Canonical Allele Identifier: CA7866632

Gene: SLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3600990T>C , CM000678.2:g.3600990T>C	GRCh38
NC_000016.9:g.3650991T>C , CM000678.1:g.3650991T>C	GRCh37
NC_000016.8:g.3590992T>C	NCBI36
NG_028123.1:g.15595A>G , LRG_503:g.15595A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000697858.1:n.493A>G
ENST00000294008.4:c.1152A>G MANE Select	ENSP00000294008.3:p.Pro384=
ENST00000294008.3:c.1152A>G	ENSP00000294008.3:p.Pro384=
ENST00000466154.5:n.2373A>G
ENST00000486524.1:n.2706A>G
NM_032444.2:c.1152A>G , LRG_503t1:c.1152A>G	NP_115820.2:p.Pro384=
XM_011522715.1:c.1152A>G	XP_011521017.1:p.Pro384=
NM_032444.3:c.1152A>G	NP_115820.2:p.Pro384=
XM_011522715.3:c.1152A>G	XP_011521017.1:p.Pro384=
XM_017023775.2:c.-776A>G	XP_016879264.1:n.-776A>G
XM_024450471.1:c.1152A>G	XP_024306239.1:p.Pro384=
NM_032444.4:c.1152A>G MANE Select	NP_115820.2:p.Pro384=