Canonical Allele Identifier: CA2840484248
Gene: NSDHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.152867670del , CM000685.2:g.152867670del GRCh38
NC_000023.10:g.152036214del , CM000685.1:g.152036214del GRCh37
NC_000023.9:g.151786870del NCBI36
NG_009163.1:g.41704del
NG_009163.2:g.41704del

Transcript Alleles

HGVS Amino-acid Change
ENST00000370274.8:c.786del MANE Select ENSP00000359297.3:p.Lys263ArgfsTer21
ENST00000370274.7:c.786del ENSP00000359297.3:p.Lys263ArgfsTer21
ENST00000440023.5:c.786del ENSP00000391854.1:p.Lys263ArgfsTer21
NM_001129765.1:c.786del NP_001123237.1:p.Lys263ArgfsTer21
NM_015922.2:c.786del NP_057006.1:p.Lys263ArgfsTer21
XM_011531178.1:c.786del XP_011529480.1:p.Lys263ArgfsTer21
XM_011531178.2:c.786del XP_011529480.1:p.Lys263ArgfsTer21
XM_017029564.1:c.834del XP_016885053.1:p.Lys279ArgfsTer21
NM_015922.3:c.786del MANE Select NP_057006.1:p.Lys263ArgfsTer21
NM_001129765.2:c.786del NP_001123237.1:p.Lys263ArgfsTer21