Canonical Allele Identifier: CA2466152383
Gene: NSDHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.152862641G= , CM000685.2:g.152862641G= GRCh38
NC_000023.10:g.152031185G= , CM000685.1:g.152031185G= GRCh37
NC_000023.9:g.151781841G= NCBI36
NG_009163.1:g.36675G=
NG_009163.2:g.36675G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370274.8:c.460G= MANE Select ENSP00000359297.3:p.Asp154=
ENST00000370274.7:c.460G= ENSP00000359297.3:p.Asp154=
ENST00000432467.1:c.460G= ENSP00000396266.1:p.Asp154=
ENST00000440023.5:c.460G= ENSP00000391854.1:p.Asp154=
NM_001129765.1:c.460G= NP_001123237.1:p.Asp154=
NM_015922.2:c.460G= NP_057006.1:p.Asp154=
XM_011531178.1:c.460G= XP_011529480.1:p.Asp154=
XM_011531178.2:c.460G= XP_011529480.1:p.Asp154=
XM_017029564.1:c.508G= XP_016885053.1:p.Asp170=
NM_015922.3:c.460G= MANE Select NP_057006.1:p.Asp154=
NM_001129765.2:c.460G= NP_001123237.1:p.Asp154=