Canonical Allele Identifier: CA2466153876

Gene: NSDHL

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.152867515T= , CM000685.2:g.152867515T=	GRCh38
NC_000023.10:g.152036059T= , CM000685.1:g.152036059T=	GRCh37
NC_000023.9:g.151786715T=	NCBI36
NG_009163.1:g.41549T=
NG_009163.2:g.41549T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000370274.8:c.687-56T= MANE Select	ENSP00000359297.3:n.687-56T=
ENST00000370274.7:c.687-56T=	ENSP00000359297.3:n.687-56T=
ENST00000432467.1:c.687-56T=	ENSP00000396266.1:n.687-56T=
ENST00000440023.5:c.687-56T=	ENSP00000391854.1:n.687-56T=
NM_001129765.1:c.687-56T=	NP_001123237.1:n.687-56T=
NM_015922.2:c.687-56T=	NP_057006.1:n.687-56T=
XM_011531178.1:c.687-56T=	XP_011529480.1:n.687-56T=
XM_011531178.2:c.687-56T=	XP_011529480.1:n.687-56T=
XM_017029564.1:c.735-56T=	XP_016885053.1:n.735-56T=
NM_015922.3:c.687-56T= MANE Select	NP_057006.1:n.687-56T=
NM_001129765.2:c.687-56T=	NP_001123237.1:n.687-56T=