Canonical Allele Identifier: CA519182780

Gene: NSDHL

Linked Data

• MyVariant Identifiers: chrX:g.152037537C>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.152868993C>T , CM000685.2:g.152868993C>T	GRCh38
NC_000023.10:g.152037537C>T , CM000685.1:g.152037537C>T	GRCh37
NC_000023.9:g.151788193C>T	NCBI36
NG_009163.1:g.43027C>T
NG_009163.2:g.43027C>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370274.8:c.999C>T MANE Select	ENSP00000359297.3:p.Gly333=
ENST00000370274.7:c.999C>T	ENSP00000359297.3:p.Gly333=
ENST00000440023.5:c.999C>T	ENSP00000391854.1:p.Gly333=
NM_001129765.1:c.999C>T	NP_001123237.1:p.Gly333=
NM_015922.2:c.999C>T	NP_057006.1:p.Gly333=
XM_011531178.1:c.999C>T	XP_011529480.1:p.Gly333=
XM_011531178.2:c.999C>T	XP_011529480.1:p.Gly333=
XM_017029564.1:c.1047C>T	XP_016885053.1:p.Gly349=
NM_015922.3:c.999C>T MANE Select	NP_057006.1:p.Gly333=
NM_001129765.2:c.999C>T	NP_001123237.1:p.Gly333=