Canonical Allele Identifier: CA7866791
Gene: SLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3606556G>A , CM000678.2:g.3606556G>A GRCh38
NC_000016.9:g.3656557G>A , CM000678.1:g.3656557G>A GRCh37
NC_000016.8:g.3596558G>A NCBI36
NG_028123.1:g.10029C>T , LRG_503:g.10029C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000697858.1:n.19C>T
ENST00000294008.4:c.678C>T MANE Select ENSP00000294008.3:p.His226=
ENST00000294008.3:c.678C>T ENSP00000294008.3:p.His226=
ENST00000466154.5:n.973C>T
ENST00000486524.1:n.1306C>T
NM_032444.2:c.678C>T , LRG_503t1:c.678C>T NP_115820.2:p.His226=
XM_011522715.1:c.678C>T XP_011521017.1:p.His226=
NM_032444.3:c.678C>T NP_115820.2:p.His226=
XM_011522715.3:c.678C>T XP_011521017.1:p.His226=
XM_024450471.1:c.678C>T XP_024306239.1:p.His226=
NM_032444.4:c.678C>T MANE Select NP_115820.2:p.His226=