Canonical Allele Identifier: CA6872082

Gene: DHX37

Linked Data

• dbSNP Id: rs150255577
• ExAC: 12:125453224 T / TGG
• gnomAD v2: 12-125453224-T-TGG
• gnomAD v3: 12-124968678-T-TGG
• gnomAD v4: 12-124968678-T-TGG
• COSMIC: COSN20065564
• MyVariant Identifiers: chr12:g.125453224_125453225insGG (hg19) ; chr12:g.124968678_124968679insGG (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124968684_124968685dup , CM000674.2:g.124968684_124968685dup	GRCh38
NC_000012.11:g.125453230_125453231dup , CM000674.1:g.125453230_125453231dup	GRCh37
NC_000012.10:g.124019183_124019184dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308736.7:c.1294-32_1294-31dup MANE Select	ENSP00000311135.2:n.1294-32_1294-31dup
ENST00000544745.2:c.765-32_765-31dup
ENST00000679875.1:n.1366-32_1366-31dup
ENST00000308736.6:c.1294-32_1294-31dup	ENSP00000311135.2:n.1294-32_1294-31dup
ENST00000539298.1:n.1394-32_1394-31dup
ENST00000544745.1:c.655-32_655-31dup	ENSP00000439009.1:n.655-32_655-31dup
NM_032656.3:c.1294-32_1294-31dup	NP_116045.2:n.1294-32_1294-31dup
XM_005253590.2:c.1294-32_1294-31dup	XP_005253647.1:n.1294-32_1294-31dup
XM_011538597.1:c.1294-32_1294-31dup	XP_011536899.1:n.1294-32_1294-31dup
XM_011538598.1:c.1294-32_1294-31dup	XP_011536900.1:n.1294-32_1294-31dup
XM_011538599.1:c.1294-32_1294-31dup	XP_011536901.1:n.1294-32_1294-31dup
XM_011538600.1:c.1294-32_1294-31dup	XP_011536902.1:n.1294-32_1294-31dup
XM_005253590.3:c.1294-32_1294-31dup	XP_005253647.1:n.1294-32_1294-31dup
XM_011538598.2:c.1294-32_1294-31dup	XP_011536900.1:n.1294-32_1294-31dup
XM_011538600.2:c.1294-32_1294-31dup	XP_011536902.1:n.1294-32_1294-31dup
XR_001748819.1:n.1397-32_1397-31dup
XR_001748820.1:n.1397-32_1397-31dup
NM_032656.4:c.1294-32_1294-31dup MANE Select	NP_116045.2:n.1294-32_1294-31dup