Canonical Allele Identifier: CA2466152477

Gene: NSDHL

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.152862998C= , CM000685.2:g.152862998C=	GRCh38
NC_000023.10:g.152031542C= , CM000685.1:g.152031542C=	GRCh37
NC_000023.9:g.151782198C=	NCBI36
NG_009163.1:g.37032C=
NG_009163.2:g.37032C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370274.8:c.543+274C= MANE Select	ENSP00000359297.3:n.543+274C=
ENST00000370274.7:c.543+274C=	ENSP00000359297.3:n.543+274C=
ENST00000432467.1:c.543+274C=	ENSP00000396266.1:n.543+274C=
ENST00000440023.5:c.543+274C=	ENSP00000391854.1:n.543+274C=
NM_001129765.1:c.543+274C=	NP_001123237.1:n.543+274C=
NM_015922.2:c.543+274C=	NP_057006.1:n.543+274C=
XM_011531178.1:c.543+274C=	XP_011529480.1:n.543+274C=
XM_011531178.2:c.543+274C=	XP_011529480.1:n.543+274C=
XM_017029564.1:c.591+274C=	XP_016885053.1:n.591+274C=
NM_015922.3:c.543+274C= MANE Select	NP_057006.1:n.543+274C=
NM_001129765.2:c.543+274C=	NP_001123237.1:n.543+274C=