Canonical Allele Identifier: CA2270407662
Gene: DDX5 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000017.11:g.64500556T= , CM000679.2:g.64500556T= GRCh38
NC_000017.10:g.62496674T= , CM000679.1:g.62496674T= GRCh37
NC_000017.9:g.59927136T= NCBI36
NG_013029.1:g.1511A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000225792.10:c.1434A= MANE Select ENSP00000225792.5:p.Arg478=
ENST00000450599.7:c.1434A= ENSP00000403085.3:p.Arg478=
ENST00000577922.6:c.1434A= ENSP00000464337.2:p.Arg478=
ENST00000578491.2:n.2954A=
ENST00000579461.2:n.3509A=
ENST00000580026.6:n.2831A=
ENST00000582326.2:n.4420A=
ENST00000583212.2:c.1119A= ENSP00000463903.2:p.Arg373=
ENST00000585111.2:c.1434A= ENSP00000463168.2:p.Arg478=
ENST00000585317.2:n.3641A=
ENST00000676575.1:n.2954A=
ENST00000676581.1:c.*184A= ENSP00000504407.1:n.*184A=
ENST00000676601.1:c.*449A= ENSP00000504708.1:n.*449A=
ENST00000676785.1:c.1434A= ENSP00000504794.1:p.Arg478=
ENST00000676969.1:n.2206A=
ENST00000677726.1:c.*1049A= ENSP00000504260.1:n.*1049A=
ENST00000678110.1:n.3131A=
ENST00000678757.1:c.*184A= ENSP00000504731.1:n.*184A=
ENST00000678810.1:n.3265A=
ENST00000678814.1:c.*270A= ENSP00000503045.1:n.*270A=
ENST00000678890.1:n.3458A=
ENST00000225792.9:c.1434A= ENSP00000225792.5:p.Arg478=
ENST00000450599.6:c.1197A= ENSP00000403085.2:p.Arg399=
ENST00000540698.6:c.*1046A= ENSP00000440276.2:n.*1046A=
ENST00000578758.5:n.467A=
ENST00000578804.5:c.1434A= ENSP00000462885.1:p.Arg478=
ENST00000580026.5:n.947A=
ENST00000581230.5:n.2840A=
ENST00000581237.2:n.443A=
ENST00000581693.5:c.*1151A= ENSP00000464566.1:n.*1151A=
NM_004396.3:c.1434A= NP_004387.1:p.Arg478=
XM_005257111.1:c.1434A= XP_005257168.1:p.Arg478=
XM_006721738.1:c.1434A= XP_006721801.1:p.Arg478=
XM_011524456.1:c.1434A= XP_011522758.1:p.Arg478=
XM_011524457.1:c.1217-230A= XP_011522759.1:n.1217-230A=
NM_001320595.1:c.1434A= NP_001307524.1:p.Arg478=
NM_001320596.2:c.1434A= NP_001307525.1:p.Arg478=
NM_001320597.1:c.1434A= NP_001307526.1:p.Arg478=
NM_004396.4:c.1434A= NP_004387.1:p.Arg478=
NM_001320595.2:c.1434A= NP_001307524.1:p.Arg478=
NM_001320597.2:c.1434A= NP_001307526.1:p.Arg478=
NM_004396.5:c.1434A= MANE Select NP_004387.1:p.Arg478=
NM_001320596.3:c.1434A= NP_001307525.1:p.Arg478=