Canonical Allele Identifier: CA394520080
Gene: SLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3590174A>C , CM000678.2:g.3590174A>C GRCh38
NC_000016.9:g.3640175A>C , CM000678.1:g.3640175A>C GRCh37
NC_000016.8:g.3580176A>C NCBI36
NG_028123.1:g.26411T>G , LRG_503:g.26411T>G

Transcript Alleles

HGVS Amino-acid Change
NM_032444.4:c.3464T>G MANE Select NP_115820.2:p.Leu1155Arg
ENST00000294008.4:c.3464T>G MANE Select ENSP00000294008.3:p.Leu1155Arg
NM_032444.2:c.3464T>G , LRG_503t1:c.3464T>G NP_115820.2:p.Leu1155Arg
NM_032444.3:c.3464T>G NP_115820.2:p.Leu1155Arg
ENST00000294008.3:c.3464T>G ENSP00000294008.3:p.Leu1155Arg
XM_011522715.1:c.3464T>G XP_011521017.1:p.Leu1155Arg
XM_011522715.3:c.3464T>G XP_011521017.1:p.Leu1155Arg
XM_017023775.2:c.2642T>G XP_016879264.1:p.Leu881Arg
XM_024450471.1:c.3464T>G XP_024306239.1:p.Leu1155Arg