Canonical Allele Identifier: CA394520072
Gene: SLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3590170G>C , CM000678.2:g.3590170G>C GRCh38
NC_000016.9:g.3640171G>C , CM000678.1:g.3640171G>C GRCh37
NC_000016.8:g.3580172G>C NCBI36
NG_028123.1:g.26415C>G , LRG_503:g.26415C>G

Transcript Alleles

HGVS Amino-acid Change
NM_032444.4:c.3468C>G MANE Select NP_115820.2:p.Asp1156Glu
ENST00000294008.4:c.3468C>G MANE Select ENSP00000294008.3:p.Asp1156Glu
NM_032444.2:c.3468C>G , LRG_503t1:c.3468C>G NP_115820.2:p.Asp1156Glu
NM_032444.3:c.3468C>G NP_115820.2:p.Asp1156Glu
ENST00000294008.3:c.3468C>G ENSP00000294008.3:p.Asp1156Glu
XM_011522715.1:c.3468C>G XP_011521017.1:p.Asp1156Glu
XM_011522715.3:c.3468C>G XP_011521017.1:p.Asp1156Glu
XM_017023775.2:c.2646C>G XP_016879264.1:p.Asp882Glu
XM_024450471.1:c.3468C>G XP_024306239.1:p.Asp1156Glu