Canonical Allele Identifier: CA482291532

Gene: DHX37

Linked Data

• MyVariant Identifiers: chr12:g.125453174T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124968628T>C , CM000674.2:g.124968628T>C	GRCh38
NC_000012.11:g.125453174T>C , CM000674.1:g.125453174T>C	GRCh37
NC_000012.10:g.124019127T>C	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308736.7:c.1314A>G MANE Select	ENSP00000311135.2:p.Pro438=
ENST00000544745.2:c.785A>G
ENST00000679875.1:n.1386A>G
ENST00000308736.6:c.1314A>G	ENSP00000311135.2:p.Pro438=
ENST00000539298.1:n.1414A>G
ENST00000544745.1:c.675A>G	ENSP00000439009.1:p.Pro225=
NM_032656.3:c.1314A>G	NP_116045.2:p.Pro438=
XM_005253590.2:c.1314A>G	XP_005253647.1:p.Pro438=
XM_011538597.1:c.1314A>G	XP_011536899.1:p.Pro438=
XM_011538598.1:c.1314A>G	XP_011536900.1:p.Pro438=
XM_011538599.1:c.1314A>G	XP_011536901.1:p.Pro438=
XM_011538600.1:c.1314A>G	XP_011536902.1:p.Pro438=
XM_005253590.3:c.1314A>G	XP_005253647.1:p.Pro438=
XM_011538598.2:c.1314A>G	XP_011536900.1:p.Pro438=
XM_011538600.2:c.1314A>G	XP_011536902.1:p.Pro438=
XR_001748819.1:n.1417A>G
XR_001748820.1:n.1417A>G
NM_032656.4:c.1314A>G MANE Select	NP_116045.2:p.Pro438=