Canonical Allele Identifier: CA387226074

Gene: DHX37

Linked Data

• MyVariant Identifiers: chr12:g.125453178A>T (hg19) ; chr12:g.124968632A>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124968632A>T , CM000674.2:g.124968632A>T	GRCh38
NC_000012.11:g.125453178A>T , CM000674.1:g.125453178A>T	GRCh37
NC_000012.10:g.124019131A>T	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308736.7:c.1310T>A MANE Select	ENSP00000311135.2:p.Phe437Tyr
ENST00000544745.2:c.781T>A
ENST00000679875.1:n.1382T>A
ENST00000308736.6:c.1310T>A	ENSP00000311135.2:p.Phe437Tyr
ENST00000539298.1:n.1410T>A
ENST00000544745.1:c.671T>A	ENSP00000439009.1:p.Phe224Tyr
NM_032656.3:c.1310T>A	NP_116045.2:p.Phe437Tyr
XM_005253590.2:c.1310T>A	XP_005253647.1:p.Phe437Tyr
XM_011538597.1:c.1310T>A	XP_011536899.1:p.Phe437Tyr
XM_011538598.1:c.1310T>A	XP_011536900.1:p.Phe437Tyr
XM_011538599.1:c.1310T>A	XP_011536901.1:p.Phe437Tyr
XM_011538600.1:c.1310T>A	XP_011536902.1:p.Phe437Tyr
XM_005253590.3:c.1310T>A	XP_005253647.1:p.Phe437Tyr
XM_011538598.2:c.1310T>A	XP_011536900.1:p.Phe437Tyr
XM_011538600.2:c.1310T>A	XP_011536902.1:p.Phe437Tyr
XR_001748819.1:n.1413T>A
XR_001748820.1:n.1413T>A
NM_032656.4:c.1310T>A MANE Select	NP_116045.2:p.Phe437Tyr