Canonical Allele Identifier: CA2621783136

Gene: DHX37

Linked Data

• gnomAD v4: 12-124968563-AC-A

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124968565del , CM000674.2:g.124968565del	GRCh38
NC_000012.11:g.125453111del , CM000674.1:g.125453111del	GRCh37
NC_000012.10:g.124019064del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308736.7:c.1378del MANE Select	ENSP00000311135.2:p.Val460SerfsTer17
ENST00000544745.2:c.849del
ENST00000679875.1:n.1450del
ENST00000308736.6:c.1378del	ENSP00000311135.2:p.Val460SerfsTer17
ENST00000539298.1:n.1478del
ENST00000544745.1:c.739del	ENSP00000439009.1:p.Val247SerfsTer17
NM_032656.3:c.1378del	NP_116045.2:p.Val460SerfsTer17
XM_005253590.2:c.1378del	XP_005253647.1:p.Val460SerfsTer17
XM_011538597.1:c.1378del	XP_011536899.1:p.Val460SerfsTer17
XM_011538598.1:c.1378del	XP_011536900.1:p.Val460SerfsTer17
XM_011538599.1:c.1378del	XP_011536901.1:p.Val460SerfsTer17
XM_011538600.1:c.1378del	XP_011536902.1:p.Val460SerfsTer17
XM_005253590.3:c.1378del	XP_005253647.1:p.Val460SerfsTer17
XM_011538598.2:c.1378del	XP_011536900.1:p.Val460SerfsTer17
XM_011538600.2:c.1378del	XP_011536902.1:p.Val460SerfsTer17
XR_001748819.1:n.1481del
XR_001748820.1:n.1481del
NM_032656.4:c.1378del MANE Select	NP_116045.2:p.Val460SerfsTer17