Canonical Allele Identifier: CA684821087

Gene: DHX37

Linked Data

• dbSNP Id: rs1370477765
• gnomAD v3: 12-124968419-TG-T
• gnomAD v4: 12-124968419-TG-T
• MyVariant Identifiers: chr12:g.125452966del (hg19) ; chr12:g.124968420del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124968421del , CM000674.2:g.124968421del	GRCh38
NC_000012.11:g.125452967del , CM000674.1:g.125452967del	GRCh37
NC_000012.10:g.124018920del	NCBI36

Transcript Alleles

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