Canonical Allele Identifier: CA2069577281
Gene: DHX37 HGNC NCBI

Linked Data

dbSNP Id: rs1954461507

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.124969009_124969011dup , CM000674.2:g.124969009_124969011dup GRCh38
NC_000012.11:g.125453555_125453557dup , CM000674.1:g.125453555_125453557dup GRCh37
NC_000012.10:g.124019508_124019510dup NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000308736.7:c.1192-42_1192-40dup MANE Select ENSP00000311135.2:n.1192-42_1192-40dup
ENST00000544745.2:c.663-42_663-40dup
ENST00000679875.1:n.1264-42_1264-40dup
ENST00000308736.6:c.1192-42_1192-40dup ENSP00000311135.2:n.1192-42_1192-40dup
ENST00000539298.1:n.1292-42_1292-40dup
ENST00000544745.1:c.553-42_553-40dup ENSP00000439009.1:n.553-42_553-40dup
NM_032656.3:c.1192-42_1192-40dup NP_116045.2:n.1192-42_1192-40dup
XM_005253590.2:c.1192-42_1192-40dup XP_005253647.1:n.1192-42_1192-40dup
XM_011538597.1:c.1192-42_1192-40dup XP_011536899.1:n.1192-42_1192-40dup
XM_011538598.1:c.1192-42_1192-40dup XP_011536900.1:n.1192-42_1192-40dup
XM_011538599.1:c.1192-42_1192-40dup XP_011536901.1:n.1192-42_1192-40dup
XM_011538600.1:c.1192-42_1192-40dup XP_011536902.1:n.1192-42_1192-40dup
XM_005253590.3:c.1192-42_1192-40dup XP_005253647.1:n.1192-42_1192-40dup
XM_011538598.2:c.1192-42_1192-40dup XP_011536900.1:n.1192-42_1192-40dup
XM_011538600.2:c.1192-42_1192-40dup XP_011536902.1:n.1192-42_1192-40dup
XR_001748819.1:n.1295-42_1295-40dup
XR_001748820.1:n.1295-42_1295-40dup
NM_032656.4:c.1192-42_1192-40dup MANE Select NP_116045.2:n.1192-42_1192-40dup