Canonical Allele Identifier: CA7866500

Gene: SLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3597551G>C , CM000678.2:g.3597551G>C	GRCh38
NC_000016.9:g.3647552G>C , CM000678.1:g.3647552G>C	GRCh37
NC_000016.8:g.3587553G>C	NCBI36
NG_028123.1:g.19034C>G , LRG_503:g.19034C>G

Transcript Alleles

HGVS	Amino-acid Change
NM_032444.4:c.1511C>G MANE Select	NP_115820.2:p.Pro504Arg
ENST00000294008.4:c.1511C>G MANE Select	ENSP00000294008.3:p.Pro504Arg
NM_032444.2:c.1511C>G , LRG_503t1:c.1511C>G	NP_115820.2:p.Pro504Arg
NM_032444.3:c.1511C>G	NP_115820.2:p.Pro504Arg
ENST00000294008.3:c.1511C>G	ENSP00000294008.3:p.Pro504Arg
ENST00000466154.5:n.2732C>G
XM_011522715.1:c.1511C>G	XP_011521017.1:p.Pro504Arg
XM_011522715.3:c.1511C>G	XP_011521017.1:p.Pro504Arg
XM_017023775.2:c.689C>G	XP_016879264.1:p.Pro230Arg
XM_024450471.1:c.1511C>G	XP_024306239.1:p.Pro504Arg