Canonical Allele Identifier: CA352590426
Gene: DHX30 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.47848259G>A , CM000665.2:g.47848259G>A GRCh38
NC_000003.11:g.47889749G>A , CM000665.1:g.47889749G>A GRCh37
NC_000003.10:g.47864753G>A NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000445061.6:c.2366G>A MANE Select ENSP00000405620.1:p.Gly789Asp
ENST00000348968.8:c.2282G>A ENSP00000343442.4:p.Gly761Asp
ENST00000395745.6:c.*2266G>A ENSP00000379094.2:n.*2266G>A
ENST00000445061.5:c.2366G>A ENSP00000405620.1:p.Gly789Asp
ENST00000446256.6:c.2366G>A ENSP00000392601.3:p.Gly789Asp
ENST00000457607.1:c.2450G>A ENSP00000394682.1:p.Gly817Asp
ENST00000474183.1:n.483G>A
ENST00000619982.4:c.2249G>A ENSP00000483160.1:p.Gly750Asp
NM_014966.3:c.2249G>A NP_055781.2:p.Gly750Asp
NM_138615.2:c.2366G>A NP_619520.1:p.Gly789Asp
XM_006713033.1:c.2270G>A XP_006713096.1:p.Gly757Asp
XM_011533490.1:c.2579G>A XP_011531792.1:p.Gly860Asp
XM_011533491.1:c.2579G>A XP_011531793.1:p.Gly860Asp
XM_011533492.1:c.2579G>A XP_011531794.1:p.Gly860Asp
XM_011533493.1:c.2468G>A XP_011531795.1:p.Gly823Asp
XM_011533494.1:c.2366G>A XP_011531796.1:p.Gly789Asp
XM_011533495.1:c.2366G>A XP_011531797.1:p.Gly789Asp
XM_011533496.1:c.2282G>A XP_011531798.1:p.Gly761Asp
XM_011533497.1:c.2282G>A XP_011531799.1:p.Gly761Asp
XM_011533498.1:c.2282G>A XP_011531800.1:p.Gly761Asp
NM_001330990.1:c.2282G>A NP_001317919.1:p.Gly761Asp
XM_011533490.2:c.2579G>A XP_011531792.1:p.Gly860Asp
XM_011533494.3:c.2366G>A XP_011531796.1:p.Gly789Asp
XM_011533495.2:c.2366G>A XP_011531797.1:p.Gly789Asp
XM_011533497.2:c.2282G>A XP_011531799.1:p.Gly761Asp
XM_017005914.1:c.2498G>A XP_016861403.1:p.Gly833Asp
XM_017005915.1:c.2270G>A XP_016861404.1:p.Gly757Asp
XM_017005916.2:c.2255G>A XP_016861405.1:p.Gly752Asp
XM_017005917.1:c.2249G>A XP_016861406.1:p.Gly750Asp
XM_024453405.1:c.2468G>A XP_024309173.1:p.Gly823Asp
NM_138615.3:c.2366G>A MANE Select NP_619520.1:p.Gly789Asp
NM_001330990.2:c.2282G>A NP_001317919.1:p.Gly761Asp
NM_014966.4:c.2249G>A NP_055781.2:p.Gly750Asp