Canonical Allele Identifier: CA2069576528

Gene: DHX37

Linked Data

• dbSNP Id: rs1954452931

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124968798del , CM000674.2:g.124968798del	GRCh38
NC_000012.11:g.125453344del , CM000674.1:g.125453344del	GRCh37
NC_000012.10:g.124019297del	NCBI36

Transcript Alleles

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