Canonical Allele Identifier: CA2579725459
Gene: NSDHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.152862558del , CM000685.2:g.152862558del GRCh38
NC_000023.10:g.152031102del , CM000685.1:g.152031102del GRCh37
NC_000023.9:g.151781758del NCBI36
NG_009163.1:g.36592del
NG_009163.2:g.36592del

Transcript Alleles

HGVS Amino-acid change
ENST00000370274.8:c.415-38del MANE Select ENSP00000359297.3:n.415-38del
ENST00000370274.7:c.415-38del ENSP00000359297.3:n.415-38del
ENST00000432467.1:c.415-38del ENSP00000396266.1:n.415-38del
ENST00000440023.5:c.415-38del ENSP00000391854.1:n.415-38del
NM_001129765.1:c.415-38del NP_001123237.1:n.415-38del
NM_015922.2:c.415-38del NP_057006.1:n.415-38del
XM_011531178.1:c.415-38del XP_011529480.1:n.415-38del
XM_011531178.2:c.415-38del XP_011529480.1:n.415-38del
XM_017029564.1:c.463-38del XP_016885053.1:n.463-38del
NM_015922.3:c.415-38del MANE Select NP_057006.1:n.415-38del
NM_001129765.2:c.415-38del NP_001123237.1:n.415-38del