Canonical Allele Identifier: CA7865437

Gene: SLX4

Genomic Alleles

HGVS	Genome Assembly
NC_000016.10:g.3583190G>C , CM000678.2:g.3583190G>C	GRCh38
NC_000016.9:g.3633191G>C , CM000678.1:g.3633191G>C	GRCh37
NC_000016.8:g.3573192G>C	NCBI36
NG_028123.1:g.33395C>G , LRG_503:g.33395C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000294008.4:c.5060C>G MANE Select	ENSP00000294008.3:p.Pro1687Arg
ENST00000294008.3:c.5060C>G	ENSP00000294008.3:p.Pro1687Arg
NM_032444.2:c.5060C>G , LRG_503t1:c.5060C>G	NP_115820.2:p.Pro1687Arg
XM_011522715.1:c.5057C>G	XP_011521017.1:p.Pro1686Arg
NM_032444.3:c.5060C>G	NP_115820.2:p.Pro1687Arg
XM_011522715.3:c.5057C>G	XP_011521017.1:p.Pro1686Arg
XM_017023775.2:c.4238C>G	XP_016879264.1:p.Pro1413Arg
XM_024450471.1:c.5060C>G	XP_024306239.1:p.Pro1687Arg
NM_032444.4:c.5060C>G MANE Select	NP_115820.2:p.Pro1687Arg