Canonical Allele Identifier: CA2797852686

Gene: DHX37

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124968595_124968596insGCTGGAAGACTACAGTGGCGAGTGCTTCCTTCCGGAAGCACTCGCCACTGTAGTCTTCC , CM000674.2:g.124968595_124968596insGCTGGAAGACTACAGTGGCGAGTGCTTCCTTCCGGAAGCACTCGCCACTGTAGTCTTCC	GRCh38
NC_000012.11:g.125453141_125453142insGCTGGAAGACTACAGTGGCGAGTGCTTCCTTCCGGAAGCACTCGCCACTGTAGTCTTCC , CM000674.1:g.125453141_125453142insGCTGGAAGACTACAGTGGCGAGTGCTTCCTTCCGGAAGCACTCGCCACTGTAGTCTTCC	GRCh37
NC_000012.10:g.124019094_124019095insGCTGGAAGACTACAGTGGCGAGTGCTTCCTTCCGGAAGCACTCGCCACTGTAGTCTTCC	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308736.7:c.1378_1379insAAGCACTCGCCACTGTAGTCTTCCAGCGGAAGACTACAGTGGCGAGTGCTTCCGGAAGG MANE Select	ENSP00000311135.2:p.Val460GlufsTer37
ENST00000544745.2:c.849_850insAAGCACTCGCCACTGTAGTCTTCCAGCGGAAGACTACAGTGGCGAGTGCTTCCGGAAGG
ENST00000679875.1:n.1450_1451insAAGCACTCGCCACTGTAGTCTTCCAGCGGAAGACTACAGTGGCGAGTGCTTCCGGAAGG
ENST00000308736.6:c.1378_1379insAAGCACTCGCCACTGTAGTCTTCCAGCGGAAGACTACAGTGGCGAGTGCTTCCGGAAGG	ENSP00000311135.2:p.Val460GlufsTer37
ENST00000539298.1:n.1478_1479insAAGCACTCGCCACTGTAGTCTTCCAGCGGAAGACTACAGTGGCGAGTGCTTCCGGAAGG
ENST00000544745.1:c.739_740insAAGCACTCGCCACTGTAGTCTTCCAGCGGAAGACTACAGTGGCGAGTGCTTCCGGAAGG	ENSP00000439009.1:p.Val247GlufsTer37
NM_032656.3:c.1378_1379insAAGCACTCGCCACTGTAGTCTTCCAGCGGAAGACTACAGTGGCGAGTGCTTCCGGAAGG	NP_116045.2:p.Val460GlufsTer37
XM_005253590.2:c.1378_1379insAAGCACTCGCCACTGTAGTCTTCCAGCGGAAGACTACAGTGGCGAGTGCTTCCGGAAGG	XP_005253647.1:p.Val460GlufsTer37
XM_011538597.1:c.1378_1379insAAGCACTCGCCACTGTAGTCTTCCAGCGGAAGACTACAGTGGCGAGTGCTTCCGGAAGG	XP_011536899.1:p.Val460GlufsTer37
XM_011538598.1:c.1378_1379insAAGCACTCGCCACTGTAGTCTTCCAGCGGAAGACTACAGTGGCGAGTGCTTCCGGAAGG	XP_011536900.1:p.Val460GlufsTer37
XM_011538599.1:c.1378_1379insAAGCACTCGCCACTGTAGTCTTCCAGCGGAAGACTACAGTGGCGAGTGCTTCCGGAAGG	XP_011536901.1:p.Val460GlufsTer37
XM_011538600.1:c.1378_1379insAAGCACTCGCCACTGTAGTCTTCCAGCGGAAGACTACAGTGGCGAGTGCTTCCGGAAGG	XP_011536902.1:p.Val460GlufsTer37
XM_005253590.3:c.1378_1379insAAGCACTCGCCACTGTAGTCTTCCAGCGGAAGACTACAGTGGCGAGTGCTTCCGGAAGG	XP_005253647.1:p.Val460GlufsTer37
XM_011538598.2:c.1378_1379insAAGCACTCGCCACTGTAGTCTTCCAGCGGAAGACTACAGTGGCGAGTGCTTCCGGAAGG	XP_011536900.1:p.Val460GlufsTer37
XM_011538600.2:c.1378_1379insAAGCACTCGCCACTGTAGTCTTCCAGCGGAAGACTACAGTGGCGAGTGCTTCCGGAAGG	XP_011536902.1:p.Val460GlufsTer37
XR_001748819.1:n.1481_1482insAAGCACTCGCCACTGTAGTCTTCCAGCGGAAGACTACAGTGGCGAGTGCTTCCGGAAGG
XR_001748820.1:n.1481_1482insAAGCACTCGCCACTGTAGTCTTCCAGCGGAAGACTACAGTGGCGAGTGCTTCCGGAAGG
NM_032656.4:c.1378_1379insAAGCACTCGCCACTGTAGTCTTCCAGCGGAAGACTACAGTGGCGAGTGCTTCCGGAAGG MANE Select	NP_116045.2:p.Val460GlufsTer37