Canonical Allele Identifier: CA2069576507

Gene: DHX37

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124968797_124968798delinsCA , CM000674.2:g.124968797_124968798delinsCA	GRCh38
NC_000012.11:g.125453343_125453344delinsCA , CM000674.1:g.125453343_125453344delinsCA	GRCh37
NC_000012.10:g.124019296_124019297delinsCA	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308736.7:c.1293+69_1293+70delinsTG MANE Select	ENSP00000311135.2:n.1293+69_1293+70delinsTG
ENST00000544745.2:c.764+69_764+70delinsTG
ENST00000679875.1:n.1365+69_1365+70delinsTG
ENST00000308736.6:c.1293+69_1293+70delinsTG	ENSP00000311135.2:n.1293+69_1293+70delinsTG
ENST00000539298.1:n.1393+69_1393+70delinsTG
ENST00000544745.1:c.654+69_654+70delinsTG	ENSP00000439009.1:n.654+69_654+70delinsTG
NM_032656.3:c.1293+69_1293+70delinsTG	NP_116045.2:n.1293+69_1293+70delinsTG
XM_005253590.2:c.1293+69_1293+70delinsTG	XP_005253647.1:n.1293+69_1293+70delinsTG
XM_011538597.1:c.1293+69_1293+70delinsTG	XP_011536899.1:n.1293+69_1293+70delinsTG
XM_011538598.1:c.1293+69_1293+70delinsTG	XP_011536900.1:n.1293+69_1293+70delinsTG
XM_011538599.1:c.1293+69_1293+70delinsTG	XP_011536901.1:n.1293+69_1293+70delinsTG
XM_011538600.1:c.1293+69_1293+70delinsTG	XP_011536902.1:n.1293+69_1293+70delinsTG
XM_005253590.3:c.1293+69_1293+70delinsTG	XP_005253647.1:n.1293+69_1293+70delinsTG
XM_011538598.2:c.1293+69_1293+70delinsTG	XP_011536900.1:n.1293+69_1293+70delinsTG
XM_011538600.2:c.1293+69_1293+70delinsTG	XP_011536902.1:n.1293+69_1293+70delinsTG
XR_001748819.1:n.1396+69_1396+70delinsTG
XR_001748820.1:n.1396+69_1396+70delinsTG
NM_032656.4:c.1293+69_1293+70delinsTG MANE Select	NP_116045.2:n.1293+69_1293+70delinsTG