Canonical Allele Identifier: CA2839542393
Gene: DHX30 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.47848300del , CM000665.2:g.47848300del GRCh38
NC_000003.11:g.47889790del , CM000665.1:g.47889790del GRCh37
NC_000003.10:g.47864794del NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000445061.6:c.2407del MANE Select ENSP00000405620.1:p.Met803TrpfsTer?
ENST00000348968.8:c.2323del ENSP00000343442.4:p.Met775TrpfsTer?
ENST00000395745.6:c.*2307del ENSP00000379094.2:n.*2307del
ENST00000445061.5:c.2407del ENSP00000405620.1:p.Met803TrpfsTer?
ENST00000446256.6:c.2407del ENSP00000392601.3:p.Met803TrpfsTer?
ENST00000457607.1:c.2491del ENSP00000394682.1:p.Met831TrpfsTer?
ENST00000474183.1:n.524del
ENST00000619982.4:c.2290del ENSP00000483160.1:p.Met764TrpfsTer?
NM_014966.3:c.2290del NP_055781.2:p.Met764TrpfsTer?
NM_138615.2:c.2407del NP_619520.1:p.Met803TrpfsTer?
XM_006713033.1:c.2311del XP_006713096.1:p.Met771TrpfsTer?
XM_011533490.1:c.2620del XP_011531792.1:p.Met874TrpfsTer?
XM_011533491.1:c.2620del XP_011531793.1:p.Met874TrpfsTer?
XM_011533492.1:c.2620del XP_011531794.1:p.Met874TrpfsTer?
XM_011533493.1:c.2509del XP_011531795.1:p.Met837TrpfsTer?
XM_011533494.1:c.2407del XP_011531796.1:p.Met803TrpfsTer?
XM_011533495.1:c.2407del XP_011531797.1:p.Met803TrpfsTer?
XM_011533496.1:c.2323del XP_011531798.1:p.Met775TrpfsTer?
XM_011533497.1:c.2323del XP_011531799.1:p.Met775TrpfsTer?
XM_011533498.1:c.2323del XP_011531800.1:p.Met775TrpfsTer?
NM_001330990.1:c.2323del NP_001317919.1:p.Met775TrpfsTer?
XM_011533490.2:c.2620del XP_011531792.1:p.Met874TrpfsTer?
XM_011533494.3:c.2407del XP_011531796.1:p.Met803TrpfsTer?
XM_011533495.2:c.2407del XP_011531797.1:p.Met803TrpfsTer?
XM_011533497.2:c.2323del XP_011531799.1:p.Met775TrpfsTer?
XM_017005914.1:c.2539del XP_016861403.1:p.Met847TrpfsTer?
XM_017005915.1:c.2311del XP_016861404.1:p.Met771TrpfsTer?
XM_017005916.2:c.2296del XP_016861405.1:p.Met766TrpfsTer?
XM_017005917.1:c.2290del XP_016861406.1:p.Met764TrpfsTer?
XM_024453405.1:c.2509del XP_024309173.1:p.Met837TrpfsTer?
NM_138615.3:c.2407del MANE Select NP_619520.1:p.Met803TrpfsTer?
NM_001330990.2:c.2323del NP_001317919.1:p.Met775TrpfsTer?
NM_014966.4:c.2290del NP_055781.2:p.Met764TrpfsTer?