Canonical Allele Identifier: CA10544745

Gene: NSDHL

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.152858808C>T , CM000685.2:g.152858808C>T	GRCh38
NC_000023.10:g.152027352C>T , CM000685.1:g.152027352C>T	GRCh37
NC_000023.9:g.151778008C>T	NCBI36
NG_009163.1:g.32842C>T
NG_009163.2:g.32842C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_015922.3:c.306C>T MANE Select	NP_057006.1:p.Phe102=
ENST00000370274.8:c.306C>T MANE Select	ENSP00000359297.3:p.Phe102=
NM_001129765.1:c.306C>T	NP_001123237.1:p.Phe102=
NM_001129765.2:c.306C>T	NP_001123237.1:p.Phe102=
NM_015922.2:c.306C>T	NP_057006.1:p.Phe102=
ENST00000370274.7:c.306C>T	ENSP00000359297.3:p.Phe102=
ENST00000432467.1:c.306C>T	ENSP00000396266.1:p.Phe102=
ENST00000440023.5:c.306C>T	ENSP00000391854.1:p.Phe102=
XM_011531178.1:c.306C>T	XP_011529480.1:p.Phe102=
XM_011531178.2:c.306C>T	XP_011529480.1:p.Phe102=
XM_017029564.1:c.354C>T	XP_016885053.1:p.Phe118=