Canonical Allele Identifier: CA2466152381
Gene: NSDHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.152862638G= , CM000685.2:g.152862638G= GRCh38
NC_000023.10:g.152031182G= , CM000685.1:g.152031182G= GRCh37
NC_000023.9:g.151781838G= NCBI36
NG_009163.1:g.36672G=
NG_009163.2:g.36672G=

Transcript Alleles

HGVS Amino-acid change
ENST00000370274.8:c.457G= MANE Select ENSP00000359297.3:p.Val153=
ENST00000370274.7:c.457G= ENSP00000359297.3:p.Val153=
ENST00000432467.1:c.457G= ENSP00000396266.1:p.Val153=
ENST00000440023.5:c.457G= ENSP00000391854.1:p.Val153=
NM_001129765.1:c.457G= NP_001123237.1:p.Val153=
NM_015922.2:c.457G= NP_057006.1:p.Val153=
XM_011531178.1:c.457G= XP_011529480.1:p.Val153=
XM_011531178.2:c.457G= XP_011529480.1:p.Val153=
XM_017029564.1:c.505G= XP_016885053.1:p.Val169=
NM_015922.3:c.457G= MANE Select NP_057006.1:p.Val153=
NM_001129765.2:c.457G= NP_001123237.1:p.Val153=