Canonical Allele Identifier: CA2069575598

Gene: DHX37

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124968512_124968514delinsCCT , CM000674.2:g.124968512_124968514delinsCCT	GRCh38
NC_000012.11:g.125453058_125453060delinsCCT , CM000674.1:g.125453058_125453060delinsCCT	GRCh37
NC_000012.10:g.124019011_124019013delinsCCT	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308736.7:c.1408+20_1408+22delinsAGG MANE Select	ENSP00000311135.2:n.1408+20_1408+22delinsAGG
ENST00000544745.2:c.879+20_879+22delinsAGG
ENST00000679875.1:n.1480+20_1480+22delinsAGG
ENST00000308736.6:c.1408+20_1408+22delinsAGG	ENSP00000311135.2:n.1408+20_1408+22delinsAGG
ENST00000539298.1:n.1508+20_1508+22delinsAGG
ENST00000544745.1:c.769+20_769+22delinsAGG	ENSP00000439009.1:n.769+20_769+22delinsAGG
NM_032656.3:c.1408+20_1408+22delinsAGG	NP_116045.2:n.1408+20_1408+22delinsAGG
XM_005253590.2:c.1408+20_1408+22delinsAGG	XP_005253647.1:n.1408+20_1408+22delinsAGG
XM_011538597.1:c.1408+20_1408+22delinsAGG	XP_011536899.1:n.1408+20_1408+22delinsAGG
XM_011538598.1:c.1408+20_1408+22delinsAGG	XP_011536900.1:n.1408+20_1408+22delinsAGG
XM_011538599.1:c.1408+20_1408+22delinsAGG	XP_011536901.1:n.1408+20_1408+22delinsAGG
XM_011538600.1:c.1408+20_1408+22delinsAGG	XP_011536902.1:n.1408+20_1408+22delinsAGG
XM_005253590.3:c.1408+20_1408+22delinsAGG	XP_005253647.1:n.1408+20_1408+22delinsAGG
XM_011538598.2:c.1408+20_1408+22delinsAGG	XP_011536900.1:n.1408+20_1408+22delinsAGG
XM_011538600.2:c.1408+20_1408+22delinsAGG	XP_011536902.1:n.1408+20_1408+22delinsAGG
XR_001748819.1:n.1511+20_1511+22delinsAGG
XR_001748820.1:n.1511+20_1511+22delinsAGG
NM_032656.4:c.1408+20_1408+22delinsAGG MANE Select	NP_116045.2:n.1408+20_1408+22delinsAGG