Canonical Allele Identifier: CA387224947

Gene: DHX37

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124964958G>A , CM000674.2:g.124964958G>A	GRCh38
NC_000012.11:g.125449504G>A , CM000674.1:g.125449504G>A	GRCh37
NC_000012.10:g.124015457G>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_032656.4:c.1784C>T MANE Select	NP_116045.2:p.Ser595Phe
ENST00000308736.7:c.1784C>T MANE Select	ENSP00000311135.2:p.Ser595Phe
NM_032656.3:c.1784C>T	NP_116045.2:p.Ser595Phe
ENST00000308736.6:c.1784C>T	ENSP00000311135.2:p.Ser595Phe
ENST00000539298.1:n.1884C>T
ENST00000543962.1:c.139C>T	ENSP00000443661.1:p.Leu47Phe
ENST00000544745.1:c.1145C>T	ENSP00000439009.1:p.Ser382Phe
ENST00000544745.2:c.1255C>T
ENST00000679875.1:n.1856C>T
XM_005253590.2:c.1784C>T	XP_005253647.1:p.Ser595Phe
XM_005253590.3:c.1784C>T	XP_005253647.1:p.Ser595Phe
XM_011538597.1:c.1784C>T	XP_011536899.1:p.Ser595Phe
XM_011538598.1:c.1784C>T	XP_011536900.1:p.Ser595Phe
XM_011538598.2:c.1784C>T	XP_011536900.1:p.Ser595Phe
XM_011538599.1:c.1784C>T	XP_011536901.1:p.Ser595Phe
XM_011538600.1:c.1784C>T	XP_011536902.1:p.Ser595Phe
XM_011538600.2:c.1784C>T	XP_011536902.1:p.Ser595Phe
XR_001748819.1:n.1887C>T
XR_001748820.1:n.1887C>T