Canonical Allele Identifier: CA387224673
Community Standard Title: NM_032656.4(DHX37):c.1877C>T (p.Ser626Leu)
Gene: DHX37 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.124964562G>A , CM000674.2:g.124964562G>A GRCh38
NC_000012.11:g.125449108G>A , CM000674.1:g.125449108G>A GRCh37
NC_000012.10:g.124015061G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
NM_032656.4:c.1877C>T MANE Select NP_116045.2:p.Ser626Leu
ENST00000308736.7:c.1877C>T MANE Select ENSP00000311135.2:p.Ser626Leu
NM_032656.3:c.1877C>T NP_116045.2:p.Ser626Leu
ENST00000308736.6:c.1877C>T ENSP00000311135.2:p.Ser626Leu
ENST00000539298.1:n.1977C>T
ENST00000543962.1:c.232C>T ENSP00000443661.1:p.Arg78Cys
ENST00000544745.1:c.1238C>T ENSP00000439009.1:p.Ser413Leu
ENST00000544745.2:c.1348C>T
ENST00000679875.1:n.1949C>T
XM_005253590.2:c.1877C>T XP_005253647.1:p.Ser626Leu
XM_005253590.3:c.1877C>T XP_005253647.1:p.Ser626Leu
XM_011538597.1:c.1877C>T XP_011536899.1:p.Ser626Leu
XM_011538598.1:c.1877C>T XP_011536900.1:p.Ser626Leu
XM_011538598.2:c.1877C>T XP_011536900.1:p.Ser626Leu
XM_011538599.1:c.1877C>T XP_011536901.1:p.Ser626Leu
XM_011538600.1:c.1877C>T XP_011536902.1:p.Ser626Leu
XM_011538600.2:c.1877C>T XP_011536902.1:p.Ser626Leu
XR_001748819.1:n.1980C>T
XR_001748820.1:n.1980C>T