Canonical Allele Identifier: CA1362750250
Gene: DHX30 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000003.12:g.47848327C= , CM000665.2:g.47848327C= GRCh38
NC_000003.11:g.47889817C= , CM000665.1:g.47889817C= GRCh37
NC_000003.10:g.47864821C= NCBI36

Transcript Alleles

HGVS Amino-acid Change
ENST00000445061.6:c.2434C= MANE Select ENSP00000405620.1:p.Leu812=
ENST00000348968.8:c.2350C= ENSP00000343442.4:p.Leu784=
ENST00000395745.6:c.*2334C= ENSP00000379094.2:n.*2334C=
ENST00000445061.5:c.2434C= ENSP00000405620.1:p.Leu812=
ENST00000446256.6:c.2434C= ENSP00000392601.3:p.Leu812=
ENST00000457607.1:c.2518C= ENSP00000394682.1:p.Leu840=
ENST00000474183.1:n.551C=
ENST00000619982.4:c.2317C= ENSP00000483160.1:p.Leu773=
NM_014966.3:c.2317C= NP_055781.2:p.Leu773=
NM_138615.2:c.2434C= NP_619520.1:p.Leu812=
XM_006713033.1:c.2338C= XP_006713096.1:p.Leu780=
XM_011533490.1:c.2647C= XP_011531792.1:p.Leu883=
XM_011533491.1:c.2647C= XP_011531793.1:p.Leu883=
XM_011533492.1:c.2647C= XP_011531794.1:p.Leu883=
XM_011533493.1:c.2536C= XP_011531795.1:p.Leu846=
XM_011533494.1:c.2434C= XP_011531796.1:p.Leu812=
XM_011533495.1:c.2434C= XP_011531797.1:p.Leu812=
XM_011533496.1:c.2350C= XP_011531798.1:p.Leu784=
XM_011533497.1:c.2350C= XP_011531799.1:p.Leu784=
XM_011533498.1:c.2350C= XP_011531800.1:p.Leu784=
NM_001330990.1:c.2350C= NP_001317919.1:p.Leu784=
XM_011533490.2:c.2647C= XP_011531792.1:p.Leu883=
XM_011533494.3:c.2434C= XP_011531796.1:p.Leu812=
XM_011533495.2:c.2434C= XP_011531797.1:p.Leu812=
XM_011533497.2:c.2350C= XP_011531799.1:p.Leu784=
XM_017005914.1:c.2566C= XP_016861403.1:p.Leu856=
XM_017005915.1:c.2338C= XP_016861404.1:p.Leu780=
XM_017005916.2:c.2323C= XP_016861405.1:p.Leu775=
XM_017005917.1:c.2317C= XP_016861406.1:p.Leu773=
XM_024453405.1:c.2536C= XP_024309173.1:p.Leu846=
NM_138615.3:c.2434C= MANE Select NP_619520.1:p.Leu812=
NM_001330990.2:c.2350C= NP_001317919.1:p.Leu784=
NM_014966.4:c.2317C= NP_055781.2:p.Leu773=