Canonical Allele Identifier: CA2069577251
Gene: DHX37 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.124969003G= , CM000674.2:g.124969003G= GRCh38
NC_000012.11:g.125453549G= , CM000674.1:g.125453549G= GRCh37
NC_000012.10:g.124019502G= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000308736.7:c.1192-35C= MANE Select ENSP00000311135.2:n.1192-35C=
ENST00000544745.2:c.663-35C=
ENST00000679875.1:n.1264-35C=
ENST00000308736.6:c.1192-35C= ENSP00000311135.2:n.1192-35C=
ENST00000539298.1:n.1292-35C=
ENST00000544745.1:c.553-35C= ENSP00000439009.1:n.553-35C=
NM_032656.3:c.1192-35C= NP_116045.2:n.1192-35C=
XM_005253590.2:c.1192-35C= XP_005253647.1:n.1192-35C=
XM_011538597.1:c.1192-35C= XP_011536899.1:n.1192-35C=
XM_011538598.1:c.1192-35C= XP_011536900.1:n.1192-35C=
XM_011538599.1:c.1192-35C= XP_011536901.1:n.1192-35C=
XM_011538600.1:c.1192-35C= XP_011536902.1:n.1192-35C=
XM_005253590.3:c.1192-35C= XP_005253647.1:n.1192-35C=
XM_011538598.2:c.1192-35C= XP_011536900.1:n.1192-35C=
XM_011538600.2:c.1192-35C= XP_011536902.1:n.1192-35C=
XR_001748819.1:n.1295-35C=
XR_001748820.1:n.1295-35C=
NM_032656.4:c.1192-35C= MANE Select NP_116045.2:n.1192-35C=