Canonical Allele Identifier: CA2466152379

Gene: NSDHL

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.152862632G= , CM000685.2:g.152862632G=	GRCh38
NC_000023.10:g.152031176G= , CM000685.1:g.152031176G=	GRCh37
NC_000023.9:g.151781832G=	NCBI36
NG_009163.1:g.36666G=
NG_009163.2:g.36666G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000370274.8:c.451G= MANE Select	ENSP00000359297.3:p.Glu151=
ENST00000370274.7:c.451G=	ENSP00000359297.3:p.Glu151=
ENST00000432467.1:c.451G=	ENSP00000396266.1:p.Glu151=
ENST00000440023.5:c.451G=	ENSP00000391854.1:p.Glu151=
NM_001129765.1:c.451G=	NP_001123237.1:p.Glu151=
NM_015922.2:c.451G=	NP_057006.1:p.Glu151=
XM_011531178.1:c.451G=	XP_011529480.1:p.Glu151=
XM_011531178.2:c.451G=	XP_011529480.1:p.Glu151=
XM_017029564.1:c.499G=	XP_016885053.1:p.Glu167=
NM_015922.3:c.451G= MANE Select	NP_057006.1:p.Glu151=
NM_001129765.2:c.451G=	NP_001123237.1:p.Glu151=