Canonical Allele Identifier: CA415287049

Gene: NSDHL

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.152868790C>T , CM000685.2:g.152868790C>T	GRCh38
NC_000023.10:g.152037334C>T , CM000685.1:g.152037334C>T	GRCh37
NC_000023.9:g.151787990C>T	NCBI36
NG_009163.1:g.42824C>T
NG_009163.2:g.42824C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015922.3:c.796C>T MANE Select	NP_057006.1:p.His266Tyr
ENST00000370274.8:c.796C>T MANE Select	ENSP00000359297.3:p.His266Tyr
NM_001129765.1:c.796C>T	NP_001123237.1:p.His266Tyr
NM_001129765.2:c.796C>T	NP_001123237.1:p.His266Tyr
NM_015922.2:c.796C>T	NP_057006.1:p.His266Tyr
ENST00000370274.7:c.796C>T	ENSP00000359297.3:p.His266Tyr
ENST00000440023.5:c.796C>T	ENSP00000391854.1:p.His266Tyr
XM_011531178.1:c.796C>T	XP_011529480.1:p.His266Tyr
XM_011531178.2:c.796C>T	XP_011529480.1:p.His266Tyr
XM_017029564.1:c.844C>T	XP_016885053.1:p.His282Tyr