Canonical Allele Identifier: CA394520292
Gene: SLX4 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000016.10:g.3590273G>C , CM000678.2:g.3590273G>C GRCh38
NC_000016.9:g.3640274G>C , CM000678.1:g.3640274G>C GRCh37
NC_000016.8:g.3580275G>C NCBI36
NG_028123.1:g.26312C>G , LRG_503:g.26312C>G

Transcript Alleles

HGVS Amino-acid Change
NM_032444.4:c.3365C>G MANE Select NP_115820.2:p.Pro1122Arg
ENST00000294008.4:c.3365C>G MANE Select ENSP00000294008.3:p.Pro1122Arg
NM_032444.2:c.3365C>G , LRG_503t1:c.3365C>G NP_115820.2:p.Pro1122Arg
NM_032444.3:c.3365C>G NP_115820.2:p.Pro1122Arg
ENST00000294008.3:c.3365C>G ENSP00000294008.3:p.Pro1122Arg
XM_011522715.1:c.3365C>G XP_011521017.1:p.Pro1122Arg
XM_011522715.3:c.3365C>G XP_011521017.1:p.Pro1122Arg
XM_017023775.2:c.2543C>G XP_016879264.1:p.Pro848Arg
XM_024450471.1:c.3365C>G XP_024306239.1:p.Pro1122Arg