Canonical Allele Identifier: CA2466153817
Gene: NSDHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.152867341G= , CM000685.2:g.152867341G= GRCh38
NC_000023.10:g.152035885G= , CM000685.1:g.152035885G= GRCh37
NC_000023.9:g.151786541G= NCBI36
NG_009163.1:g.41375G=
NG_009163.2:g.41375G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000370274.8:c.687-230G= MANE Select ENSP00000359297.3:n.687-230G=
ENST00000370274.7:c.687-230G= ENSP00000359297.3:n.687-230G=
ENST00000432467.1:c.687-230G= ENSP00000396266.1:n.687-230G=
ENST00000440023.5:c.687-230G= ENSP00000391854.1:n.687-230G=
NM_001129765.1:c.687-230G= NP_001123237.1:n.687-230G=
NM_015922.2:c.687-230G= NP_057006.1:n.687-230G=
XM_011531178.1:c.687-230G= XP_011529480.1:n.687-230G=
XM_011531178.2:c.687-230G= XP_011529480.1:n.687-230G=
XM_017029564.1:c.735-230G= XP_016885053.1:n.735-230G=
NM_015922.3:c.687-230G= MANE Select NP_057006.1:n.687-230G=
NM_001129765.2:c.687-230G= NP_001123237.1:n.687-230G=