Canonical Allele Identifier: CA394520091
Gene: SLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3590178A>T , CM000678.2:g.3590178A>T GRCh38
NC_000016.9:g.3640179A>T , CM000678.1:g.3640179A>T GRCh37
NC_000016.8:g.3580180A>T NCBI36
NG_028123.1:g.26407T>A , LRG_503:g.26407T>A

Transcript Alleles

HGVS Amino-acid Change
NM_032444.4:c.3460T>A MANE Select NP_115820.2:p.Leu1154Ile
ENST00000294008.4:c.3460T>A MANE Select ENSP00000294008.3:p.Leu1154Ile
NM_032444.2:c.3460T>A , LRG_503t1:c.3460T>A NP_115820.2:p.Leu1154Ile
NM_032444.3:c.3460T>A NP_115820.2:p.Leu1154Ile
ENST00000294008.3:c.3460T>A ENSP00000294008.3:p.Leu1154Ile
XM_011522715.1:c.3460T>A XP_011521017.1:p.Leu1154Ile
XM_011522715.3:c.3460T>A XP_011521017.1:p.Leu1154Ile
XM_017023775.2:c.2638T>A XP_016879264.1:p.Leu880Ile
XM_024450471.1:c.3460T>A XP_024306239.1:p.Leu1154Ile