Canonical Allele Identifier: CA684821571

Gene: DHX37

Linked Data

• dbSNP Id: rs1321803291
• gnomAD v3: 12-124968764-T-TG
• gnomAD v4: 12-124968764-T-TG
• MyVariant Identifiers: chr12:g.125453310_125453311insG (hg19) ; chr12:g.124968764_124968765insG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124968765dup , CM000674.2:g.124968765dup	GRCh38
NC_000012.11:g.125453311dup , CM000674.1:g.125453311dup	GRCh37
NC_000012.10:g.124019264dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308736.7:c.1293+102dup MANE Select	ENSP00000311135.2:n.1293+102dup
ENST00000544745.2:c.764+102dup
ENST00000679875.1:n.1365+102dup
ENST00000308736.6:c.1293+102dup	ENSP00000311135.2:n.1293+102dup
ENST00000539298.1:n.1393+102dup
ENST00000544745.1:c.654+102dup	ENSP00000439009.1:n.654+102dup
NM_032656.3:c.1293+102dup	NP_116045.2:n.1293+102dup
XM_005253590.2:c.1293+102dup	XP_005253647.1:n.1293+102dup
XM_011538597.1:c.1293+102dup	XP_011536899.1:n.1293+102dup
XM_011538598.1:c.1293+102dup	XP_011536900.1:n.1293+102dup
XM_011538599.1:c.1293+102dup	XP_011536901.1:n.1293+102dup
XM_011538600.1:c.1293+102dup	XP_011536902.1:n.1293+102dup
XM_005253590.3:c.1293+102dup	XP_005253647.1:n.1293+102dup
XM_011538598.2:c.1293+102dup	XP_011536900.1:n.1293+102dup
XM_011538600.2:c.1293+102dup	XP_011536902.1:n.1293+102dup
XR_001748819.1:n.1396+102dup
XR_001748820.1:n.1396+102dup
NM_032656.4:c.1293+102dup MANE Select	NP_116045.2:n.1293+102dup