Canonical Allele Identifier: CA245270805

Gene: DHX37

Linked Data

• dbSNP Id: rs565054685
• gnomAD v2: 12-125453262-T-TTTC
• gnomAD v3: 12-124968716-T-TTTC
• gnomAD v4: 12-124968716-T-TTTC
• MyVariant Identifiers: chr12:g.125453262_125453263insTTC (hg19) ; chr12:g.124968716_124968717insTTC (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124968717_124968719dup , CM000674.2:g.124968717_124968719dup	GRCh38
NC_000012.11:g.125453263_125453265dup , CM000674.1:g.125453263_125453265dup	GRCh37
NC_000012.10:g.124019216_124019218dup	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308736.7:c.1294-71_1294-69dup MANE Select	ENSP00000311135.2:n.1294-71_1294-69dup
ENST00000544745.2:c.765-71_765-69dup
ENST00000679875.1:n.1366-71_1366-69dup
ENST00000308736.6:c.1294-71_1294-69dup	ENSP00000311135.2:n.1294-71_1294-69dup
ENST00000539298.1:n.1394-71_1394-69dup
ENST00000544745.1:c.655-71_655-69dup	ENSP00000439009.1:n.655-71_655-69dup
NM_032656.3:c.1294-71_1294-69dup	NP_116045.2:n.1294-71_1294-69dup
XM_005253590.2:c.1294-71_1294-69dup	XP_005253647.1:n.1294-71_1294-69dup
XM_011538597.1:c.1294-71_1294-69dup	XP_011536899.1:n.1294-71_1294-69dup
XM_011538598.1:c.1294-71_1294-69dup	XP_011536900.1:n.1294-71_1294-69dup
XM_011538599.1:c.1294-71_1294-69dup	XP_011536901.1:n.1294-71_1294-69dup
XM_011538600.1:c.1294-71_1294-69dup	XP_011536902.1:n.1294-71_1294-69dup
XM_005253590.3:c.1294-71_1294-69dup	XP_005253647.1:n.1294-71_1294-69dup
XM_011538598.2:c.1294-71_1294-69dup	XP_011536900.1:n.1294-71_1294-69dup
XM_011538600.2:c.1294-71_1294-69dup	XP_011536902.1:n.1294-71_1294-69dup
XR_001748819.1:n.1397-71_1397-69dup
XR_001748820.1:n.1397-71_1397-69dup
NM_032656.4:c.1294-71_1294-69dup MANE Select	NP_116045.2:n.1294-71_1294-69dup