Canonical Allele Identifier: CA2069576809

Gene: DHX37

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124968874A= , CM000674.2:g.124968874A=	GRCh38
NC_000012.11:g.125453420A= , CM000674.1:g.125453420A=	GRCh37
NC_000012.10:g.124019373A=	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308736.7:c.1286T= MANE Select	ENSP00000311135.2:p.Val429=
ENST00000544745.2:c.757T=
ENST00000679875.1:n.1358T=
ENST00000308736.6:c.1286T=	ENSP00000311135.2:p.Val429=
ENST00000539298.1:n.1386T=
ENST00000544745.1:c.647T=	ENSP00000439009.1:p.Val216=
NM_032656.3:c.1286T=	NP_116045.2:p.Val429=
XM_005253590.2:c.1286T=	XP_005253647.1:p.Val429=
XM_011538597.1:c.1286T=	XP_011536899.1:p.Val429=
XM_011538598.1:c.1286T=	XP_011536900.1:p.Val429=
XM_011538599.1:c.1286T=	XP_011536901.1:p.Val429=
XM_011538600.1:c.1286T=	XP_011536902.1:p.Val429=
XM_005253590.3:c.1286T=	XP_005253647.1:p.Val429=
XM_011538598.2:c.1286T=	XP_011536900.1:p.Val429=
XM_011538600.2:c.1286T=	XP_011536902.1:p.Val429=
XR_001748819.1:n.1389T=
XR_001748820.1:n.1389T=
NM_032656.4:c.1286T= MANE Select	NP_116045.2:p.Val429=