Canonical Allele Identifier: CA2466153917

Gene: NSDHL

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.152867659A= , CM000685.2:g.152867659A=	GRCh38
NC_000023.10:g.152036203A= , CM000685.1:g.152036203A=	GRCh37
NC_000023.9:g.151786859A=	NCBI36
NG_009163.1:g.41693A=
NG_009163.2:g.41693A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370274.8:c.775A= MANE Select	ENSP00000359297.3:p.Thr259=
ENST00000370274.7:c.775A=	ENSP00000359297.3:p.Thr259=
ENST00000440023.5:c.775A=	ENSP00000391854.1:p.Thr259=
NM_001129765.1:c.775A=	NP_001123237.1:p.Thr259=
NM_015922.2:c.775A=	NP_057006.1:p.Thr259=
XM_011531178.1:c.775A=	XP_011529480.1:p.Thr259=
XM_011531178.2:c.775A=	XP_011529480.1:p.Thr259=
XM_017029564.1:c.823A=	XP_016885053.1:p.Thr275=
NM_015922.3:c.775A= MANE Select	NP_057006.1:p.Thr259=
NM_001129765.2:c.775A=	NP_001123237.1:p.Thr259=