Canonical Allele Identifier: CA482291516

Gene: DHX37

Linked Data

• MyVariant Identifiers: chr12:g.125453150C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124968604C>A , CM000674.2:g.124968604C>A	GRCh38
NC_000012.11:g.125453150C>A , CM000674.1:g.125453150C>A	GRCh37
NC_000012.10:g.124019103C>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308736.7:c.1338G>T MANE Select	ENSP00000311135.2:p.Arg446=
ENST00000544745.2:c.809G>T
ENST00000679875.1:n.1410G>T
ENST00000308736.6:c.1338G>T	ENSP00000311135.2:p.Arg446=
ENST00000539298.1:n.1438G>T
ENST00000544745.1:c.699G>T	ENSP00000439009.1:p.Arg233=
NM_032656.3:c.1338G>T	NP_116045.2:p.Arg446=
XM_005253590.2:c.1338G>T	XP_005253647.1:p.Arg446=
XM_011538597.1:c.1338G>T	XP_011536899.1:p.Arg446=
XM_011538598.1:c.1338G>T	XP_011536900.1:p.Arg446=
XM_011538599.1:c.1338G>T	XP_011536901.1:p.Arg446=
XM_011538600.1:c.1338G>T	XP_011536902.1:p.Arg446=
XM_005253590.3:c.1338G>T	XP_005253647.1:p.Arg446=
XM_011538598.2:c.1338G>T	XP_011536900.1:p.Arg446=
XM_011538600.2:c.1338G>T	XP_011536902.1:p.Arg446=
XR_001748819.1:n.1441G>T
XR_001748820.1:n.1441G>T
NM_032656.4:c.1338G>T MANE Select	NP_116045.2:p.Arg446=