Canonical Allele Identifier: CA2069575323

Gene: DHX37

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124968419_124968420delinsTG , CM000674.2:g.124968419_124968420delinsTG	GRCh38
NC_000012.11:g.125452965_125452966delinsTG , CM000674.1:g.125452965_125452966delinsTG	GRCh37
NC_000012.10:g.124018918_124018919delinsTG	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308736.7:c.1408+114_1408+115delinsCA MANE Select	ENSP00000311135.2:n.1408+114_1408+115delinsCA
ENST00000544745.2:c.879+114_879+115delinsCA
ENST00000679875.1:n.1480+114_1480+115delinsCA
ENST00000308736.6:c.1408+114_1408+115delinsCA	ENSP00000311135.2:n.1408+114_1408+115delinsCA
ENST00000539298.1:n.1508+114_1508+115delinsCA
ENST00000544745.1:c.769+114_769+115delinsCA	ENSP00000439009.1:n.769+114_769+115delinsCA
NM_032656.3:c.1408+114_1408+115delinsCA	NP_116045.2:n.1408+114_1408+115delinsCA
XM_005253590.2:c.1408+114_1408+115delinsCA	XP_005253647.1:n.1408+114_1408+115delinsCA
XM_011538597.1:c.1408+114_1408+115delinsCA	XP_011536899.1:n.1408+114_1408+115delinsCA
XM_011538598.1:c.1408+114_1408+115delinsCA	XP_011536900.1:n.1408+114_1408+115delinsCA
XM_011538599.1:c.1408+114_1408+115delinsCA	XP_011536901.1:n.1408+114_1408+115delinsCA
XM_011538600.1:c.1408+114_1408+115delinsCA	XP_011536902.1:n.1408+114_1408+115delinsCA
XM_005253590.3:c.1408+114_1408+115delinsCA	XP_005253647.1:n.1408+114_1408+115delinsCA
XM_011538598.2:c.1408+114_1408+115delinsCA	XP_011536900.1:n.1408+114_1408+115delinsCA
XM_011538600.2:c.1408+114_1408+115delinsCA	XP_011536902.1:n.1408+114_1408+115delinsCA
XR_001748819.1:n.1511+114_1511+115delinsCA
XR_001748820.1:n.1511+114_1511+115delinsCA
NM_032656.4:c.1408+114_1408+115delinsCA MANE Select	NP_116045.2:n.1408+114_1408+115delinsCA