Canonical Allele Identifier: CA7865380
Gene: SLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3582659A>G , CM000678.2:g.3582659A>G GRCh38
NC_000016.9:g.3632660A>G , CM000678.1:g.3632660A>G GRCh37
NC_000016.8:g.3572661A>G NCBI36
NG_028123.1:g.33926T>C , LRG_503:g.33926T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000294008.4:c.5188T>C MANE Select ENSP00000294008.3:p.Ser1730Pro
ENST00000294008.3:c.5188T>C ENSP00000294008.3:p.Ser1730Pro
NM_032444.2:c.5188T>C , LRG_503t1:c.5188T>C NP_115820.2:p.Ser1730Pro
XM_011522715.1:c.5185T>C XP_011521017.1:p.Ser1729Pro
NM_032444.3:c.5188T>C NP_115820.2:p.Ser1730Pro
XM_011522715.3:c.5185T>C XP_011521017.1:p.Ser1729Pro
XM_017023775.2:c.4366T>C XP_016879264.1:p.Ser1456Pro
XM_024450471.1:c.5188T>C XP_024306239.1:p.Ser1730Pro
NM_032444.4:c.5188T>C MANE Select NP_115820.2:p.Ser1730Pro