Canonical Allele Identifier: CA341090

Gene: NSDHL

Linked Data

• ClinVar Variation Id: 11426
• ClinVar RCV Id: RCV000012179 ; RCV002512978
• dbSNP Id: rs104894909
• MyVariant Identifiers: chrX:g.152027360C>T (hg19) ; chrX:g.152858816C>T (hg38)
• PubMed: PMID:10710235 ; PMID:21290788

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.152858816C>T , CM000685.2:g.152858816C>T	GRCh38
NC_000023.10:g.152027360C>T , CM000685.1:g.152027360C>T	GRCh37
NC_000023.9:g.151778016C>T	NCBI36
NG_009163.1:g.32850C>T
NG_009163.2:g.32850C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000370274.8:c.314C>T MANE Select	ENSP00000359297.3:p.Ala105Val
ENST00000370274.7:c.314C>T	ENSP00000359297.3:p.Ala105Val
ENST00000432467.1:c.314C>T	ENSP00000396266.1:p.Ala105Val
ENST00000440023.5:c.314C>T	ENSP00000391854.1:p.Ala105Val
NM_001129765.1:c.314C>T	NP_001123237.1:p.Ala105Val
NM_015922.2:c.314C>T	NP_057006.1:p.Ala105Val
XM_011531178.1:c.314C>T	XP_011529480.1:p.Ala105Val
XM_011531178.2:c.314C>T	XP_011529480.1:p.Ala105Val
XM_017029564.1:c.362C>T	XP_016885053.1:p.Ala121Val
NM_015922.3:c.314C>T MANE Select	NP_057006.1:p.Ala105Val
NM_001129765.2:c.314C>T	NP_001123237.1:p.Ala105Val