Canonical Allele Identifier: CA352590286
Gene: DHX30 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.47848226A>C , CM000665.2:g.47848226A>C GRCh38
NC_000003.11:g.47889716A>C , CM000665.1:g.47889716A>C GRCh37
NC_000003.10:g.47864720A>C NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000445061.6:c.2333A>C MANE Select ENSP00000405620.1:p.Gln778Pro
ENST00000348968.8:c.2249A>C ENSP00000343442.4:p.Gln750Pro
ENST00000395745.6:c.*2233A>C ENSP00000379094.2:n.*2233A>C
ENST00000445061.5:c.2333A>C ENSP00000405620.1:p.Gln778Pro
ENST00000446256.6:c.2333A>C ENSP00000392601.3:p.Gln778Pro
ENST00000457607.1:c.2417A>C ENSP00000394682.1:p.Gln806Pro
ENST00000474183.1:n.450A>C
ENST00000619982.4:c.2216A>C ENSP00000483160.1:p.Gln739Pro
NM_014966.3:c.2216A>C NP_055781.2:p.Gln739Pro
NM_138615.2:c.2333A>C NP_619520.1:p.Gln778Pro
XM_006713033.1:c.2237A>C XP_006713096.1:p.Gln746Pro
XM_011533490.1:c.2546A>C XP_011531792.1:p.Gln849Pro
XM_011533491.1:c.2546A>C XP_011531793.1:p.Gln849Pro
XM_011533492.1:c.2546A>C XP_011531794.1:p.Gln849Pro
XM_011533493.1:c.2435A>C XP_011531795.1:p.Gln812Pro
XM_011533494.1:c.2333A>C XP_011531796.1:p.Gln778Pro
XM_011533495.1:c.2333A>C XP_011531797.1:p.Gln778Pro
XM_011533496.1:c.2249A>C XP_011531798.1:p.Gln750Pro
XM_011533497.1:c.2249A>C XP_011531799.1:p.Gln750Pro
XM_011533498.1:c.2249A>C XP_011531800.1:p.Gln750Pro
NM_001330990.1:c.2249A>C NP_001317919.1:p.Gln750Pro
XM_011533490.2:c.2546A>C XP_011531792.1:p.Gln849Pro
XM_011533494.3:c.2333A>C XP_011531796.1:p.Gln778Pro
XM_011533495.2:c.2333A>C XP_011531797.1:p.Gln778Pro
XM_011533497.2:c.2249A>C XP_011531799.1:p.Gln750Pro
XM_017005914.1:c.2465A>C XP_016861403.1:p.Gln822Pro
XM_017005915.1:c.2237A>C XP_016861404.1:p.Gln746Pro
XM_017005916.2:c.2222A>C XP_016861405.1:p.Gln741Pro
XM_017005917.1:c.2216A>C XP_016861406.1:p.Gln739Pro
XM_024453405.1:c.2435A>C XP_024309173.1:p.Gln812Pro
NM_138615.3:c.2333A>C MANE Select NP_619520.1:p.Gln778Pro
NM_001330990.2:c.2249A>C NP_001317919.1:p.Gln750Pro
NM_014966.4:c.2216A>C NP_055781.2:p.Gln739Pro