Canonical Allele Identifier: CA415285218

Gene: NSDHL

Linked Data

• MyVariant Identifiers: chrX:g.152031188A>T (hg19) ; chrX:g.152862644A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.152862644A>T , CM000685.2:g.152862644A>T	GRCh38
NC_000023.10:g.152031188A>T , CM000685.1:g.152031188A>T	GRCh37
NC_000023.9:g.151781844A>T	NCBI36
NG_009163.1:g.36678A>T
NG_009163.2:g.36678A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000370274.8:c.463A>T MANE Select	ENSP00000359297.3:p.Ile155Phe
ENST00000370274.7:c.463A>T	ENSP00000359297.3:p.Ile155Phe
ENST00000432467.1:c.463A>T	ENSP00000396266.1:p.Ile155Phe
ENST00000440023.5:c.463A>T	ENSP00000391854.1:p.Ile155Phe
NM_001129765.1:c.463A>T	NP_001123237.1:p.Ile155Phe
NM_015922.2:c.463A>T	NP_057006.1:p.Ile155Phe
XM_011531178.1:c.463A>T	XP_011529480.1:p.Ile155Phe
XM_011531178.2:c.463A>T	XP_011529480.1:p.Ile155Phe
XM_017029564.1:c.511A>T	XP_016885053.1:p.Ile171Phe
NM_015922.3:c.463A>T MANE Select	NP_057006.1:p.Ile155Phe
NM_001129765.2:c.463A>T	NP_001123237.1:p.Ile155Phe