Canonical Allele Identifier: CA352590111
Gene: DHX30 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.47848184C>T , CM000665.2:g.47848184C>T GRCh38
NC_000003.11:g.47889674C>T , CM000665.1:g.47889674C>T GRCh37
NC_000003.10:g.47864678C>T NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000445061.6:c.2291C>T MANE Select ENSP00000405620.1:p.Ser764Phe
ENST00000348968.8:c.2207C>T ENSP00000343442.4:p.Ser736Phe
ENST00000395745.6:c.*2191C>T ENSP00000379094.2:n.*2191C>T
ENST00000445061.5:c.2291C>T ENSP00000405620.1:p.Ser764Phe
ENST00000446256.6:c.2291C>T ENSP00000392601.3:p.Ser764Phe
ENST00000457607.1:c.2375C>T ENSP00000394682.1:p.Ser792Phe
ENST00000474183.1:n.408C>T
ENST00000619982.4:c.2174C>T ENSP00000483160.1:p.Ser725Phe
NM_014966.3:c.2174C>T NP_055781.2:p.Ser725Phe
NM_138615.2:c.2291C>T NP_619520.1:p.Ser764Phe
XM_006713033.1:c.2195C>T XP_006713096.1:p.Ser732Phe
XM_011533490.1:c.2504C>T XP_011531792.1:p.Ser835Phe
XM_011533491.1:c.2504C>T XP_011531793.1:p.Ser835Phe
XM_011533492.1:c.2504C>T XP_011531794.1:p.Ser835Phe
XM_011533493.1:c.2393C>T XP_011531795.1:p.Ser798Phe
XM_011533494.1:c.2291C>T XP_011531796.1:p.Ser764Phe
XM_011533495.1:c.2291C>T XP_011531797.1:p.Ser764Phe
XM_011533496.1:c.2207C>T XP_011531798.1:p.Ser736Phe
XM_011533497.1:c.2207C>T XP_011531799.1:p.Ser736Phe
XM_011533498.1:c.2207C>T XP_011531800.1:p.Ser736Phe
NM_001330990.1:c.2207C>T NP_001317919.1:p.Ser736Phe
XM_011533490.2:c.2504C>T XP_011531792.1:p.Ser835Phe
XM_011533494.3:c.2291C>T XP_011531796.1:p.Ser764Phe
XM_011533495.2:c.2291C>T XP_011531797.1:p.Ser764Phe
XM_011533497.2:c.2207C>T XP_011531799.1:p.Ser736Phe
XM_017005914.1:c.2423C>T XP_016861403.1:p.Ser808Phe
XM_017005915.1:c.2195C>T XP_016861404.1:p.Ser732Phe
XM_017005916.2:c.2180C>T XP_016861405.1:p.Ser727Phe
XM_017005917.1:c.2174C>T XP_016861406.1:p.Ser725Phe
XM_024453405.1:c.2393C>T XP_024309173.1:p.Ser798Phe
NM_138615.3:c.2291C>T MANE Select NP_619520.1:p.Ser764Phe
NM_001330990.2:c.2207C>T NP_001317919.1:p.Ser736Phe
NM_014966.4:c.2174C>T NP_055781.2:p.Ser725Phe