Canonical Allele Identifier: CA2621785593

Gene: DHX37

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124975503_124975505del , CM000674.2:g.124975503_124975505del	GRCh38
NC_000012.11:g.125460049_125460051del , CM000674.1:g.125460049_125460051del	GRCh37
NC_000012.10:g.124026002_124026004del	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
NM_032656.4:c.896_898del MANE Select	NP_116045.2:p.Ser299del
ENST00000308736.7:c.896_898del MANE Select	ENSP00000311135.2:p.Ser299del
NM_032656.3:c.896_898del	NP_116045.2:p.Ser299del
ENST00000308736.6:c.896_898del	ENSP00000311135.2:p.Ser299del
ENST00000539298.1:n.996_998del
ENST00000544745.1:c.257_259del	ENSP00000439009.1:p.Ser86del
ENST00000544745.2:c.367_369del
ENST00000679875.1:n.968_970del
XM_005253590.2:c.896_898del	XP_005253647.1:p.Ser299del
XM_005253590.3:c.896_898del	XP_005253647.1:p.Ser299del
XM_011538597.1:c.896_898del	XP_011536899.1:p.Ser299del
XM_011538598.1:c.896_898del	XP_011536900.1:p.Ser299del
XM_011538598.2:c.896_898del	XP_011536900.1:p.Ser299del
XM_011538599.1:c.896_898del	XP_011536901.1:p.Ser299del
XM_011538600.1:c.896_898del	XP_011536902.1:p.Ser299del
XM_011538600.2:c.896_898del	XP_011536902.1:p.Ser299del
XR_001748819.1:n.999_1001del
XR_001748820.1:n.999_1001del