Canonical Allele Identifier: CA2466152359

Gene: NSDHL

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.152862537T= , CM000685.2:g.152862537T=	GRCh38
NC_000023.10:g.152031081T= , CM000685.1:g.152031081T=	GRCh37
NC_000023.9:g.151781737T=	NCBI36
NG_009163.1:g.36571T=
NG_009163.2:g.36571T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000370274.8:c.415-59T= MANE Select	ENSP00000359297.3:n.415-59T=
ENST00000370274.7:c.415-59T=	ENSP00000359297.3:n.415-59T=
ENST00000432467.1:c.415-59T=	ENSP00000396266.1:n.415-59T=
ENST00000440023.5:c.415-59T=	ENSP00000391854.1:n.415-59T=
NM_001129765.1:c.415-59T=	NP_001123237.1:n.415-59T=
NM_015922.2:c.415-59T=	NP_057006.1:n.415-59T=
XM_011531178.1:c.415-59T=	XP_011529480.1:n.415-59T=
XM_011531178.2:c.415-59T=	XP_011529480.1:n.415-59T=
XM_017029564.1:c.463-59T=	XP_016885053.1:n.463-59T=
NM_015922.3:c.415-59T= MANE Select	NP_057006.1:n.415-59T=
NM_001129765.2:c.415-59T=	NP_001123237.1:n.415-59T=