Canonical Allele Identifier: CA2466151282
Community Standard Title: NM_015922.3(NSDHL):c.370G= (p.Gly124=)
Gene: NSDHL HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000023.11:g.152858872G= , CM000685.2:g.152858872G= GRCh38
NC_000023.10:g.152027416G= , CM000685.1:g.152027416G= GRCh37
NC_000023.9:g.151778072G= NCBI36
NG_009163.1:g.32906G=
NG_009163.2:g.32906G=

Transcript Alleles

HGVS Amino-acid Change
NM_015922.3:c.370G= MANE Select NP_057006.1:p.Gly124=
ENST00000370274.8:c.370G= MANE Select ENSP00000359297.3:p.Gly124=
NM_001129765.1:c.370G= NP_001123237.1:p.Gly124=
NM_001129765.2:c.370G= NP_001123237.1:p.Gly124=
NM_015922.2:c.370G= NP_057006.1:p.Gly124=
ENST00000370274.7:c.370G= ENSP00000359297.3:p.Gly124=
ENST00000432467.1:c.370G= ENSP00000396266.1:p.Gly124=
ENST00000440023.5:c.370G= ENSP00000391854.1:p.Gly124=
XM_011531178.1:c.370G= XP_011529480.1:p.Gly124=
XM_011531178.2:c.370G= XP_011529480.1:p.Gly124=
XM_017029564.1:c.418G= XP_016885053.1:p.Gly140=