Canonical Allele Identifier: CA7866483
Community Standard Title: NM_032444.4(SLX4):c.1584C>G (p.Ser528Arg)
Gene: SLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3597478G>C , CM000678.2:g.3597478G>C GRCh38
NC_000016.9:g.3647479G>C , CM000678.1:g.3647479G>C GRCh37
NC_000016.8:g.3587480G>C NCBI36
NG_028123.1:g.19107C>G , LRG_503:g.19107C>G

Transcript Alleles

HGVS Amino-acid Change
NM_032444.4:c.1584C>G MANE Select NP_115820.2:p.Ser528Arg
ENST00000294008.4:c.1584C>G MANE Select ENSP00000294008.3:p.Ser528Arg
NM_032444.2:c.1584C>G , LRG_503t1:c.1584C>G NP_115820.2:p.Ser528Arg
NM_032444.3:c.1584C>G NP_115820.2:p.Ser528Arg
ENST00000294008.3:c.1584C>G ENSP00000294008.3:p.Ser528Arg
ENST00000466154.5:n.2805C>G
XM_011522715.1:c.1584C>G XP_011521017.1:p.Ser528Arg
XM_011522715.3:c.1584C>G XP_011521017.1:p.Ser528Arg
XM_017023775.2:c.762C>G XP_016879264.1:p.Ser254Arg
XM_024450471.1:c.1584C>G XP_024306239.1:p.Ser528Arg