Canonical Allele Identifier: CA387225888

Gene: DHX37

Linked Data

• COSMIC: COSM4039982
• MyVariant Identifiers: chr12:g.125453092T>A (hg19) ; chr12:g.124968546T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000012.12:g.124968546T>A , CM000674.2:g.124968546T>A	GRCh38
NC_000012.11:g.125453092T>A , CM000674.1:g.125453092T>A	GRCh37
NC_000012.10:g.124019045T>A	NCBI36

Transcript Alleles

HGVS	Amino-acid Change
ENST00000308736.7:c.1396A>T MANE Select	ENSP00000311135.2:p.Met466Leu
ENST00000544745.2:c.867A>T
ENST00000679875.1:n.1468A>T
ENST00000308736.6:c.1396A>T	ENSP00000311135.2:p.Met466Leu
ENST00000539298.1:n.1496A>T
ENST00000544745.1:c.757A>T	ENSP00000439009.1:p.Met253Leu
NM_032656.3:c.1396A>T	NP_116045.2:p.Met466Leu
XM_005253590.2:c.1396A>T	XP_005253647.1:p.Met466Leu
XM_011538597.1:c.1396A>T	XP_011536899.1:p.Met466Leu
XM_011538598.1:c.1396A>T	XP_011536900.1:p.Met466Leu
XM_011538599.1:c.1396A>T	XP_011536901.1:p.Met466Leu
XM_011538600.1:c.1396A>T	XP_011536902.1:p.Met466Leu
XM_005253590.3:c.1396A>T	XP_005253647.1:p.Met466Leu
XM_011538598.2:c.1396A>T	XP_011536900.1:p.Met466Leu
XM_011538600.2:c.1396A>T	XP_011536902.1:p.Met466Leu
XR_001748819.1:n.1499A>T
XR_001748820.1:n.1499A>T
NM_032656.4:c.1396A>T MANE Select	NP_116045.2:p.Met466Leu