Canonical Allele Identifier: CA2270407608

Gene: DDX5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.64500479_64500480delinsAC , CM000679.2:g.64500479_64500480delinsAC	GRCh38
NC_000017.10:g.62496597_62496598delinsAC , CM000679.1:g.62496597_62496598delinsAC	GRCh37
NC_000017.9:g.59927059_59927060delinsAC	NCBI36
NG_013029.1:g.1587_1588delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225792.10:c.1441+69_1441+70delinsGT MANE Select	ENSP00000225792.5:n.1441+69_1441+70delinsGT
ENST00000450599.7:c.1441+69_1441+70delinsGT	ENSP00000403085.3:n.1441+69_1441+70delinsGT
ENST00000577922.6:c.1441+69_1441+70delinsGT	ENSP00000464337.2:n.1441+69_1441+70delinsGT
ENST00000578491.2:n.3030_3031delinsGT
ENST00000579461.2:n.3585_3586delinsGT
ENST00000580026.6:n.2838+69_2838+70delinsGT
ENST00000582326.2:n.4496_4497delinsGT
ENST00000583212.2:c.1126+69_1126+70delinsGT	ENSP00000463903.2:n.1126+69_1126+70delinsGT
ENST00000585111.2:c.1441+69_1441+70delinsGT	ENSP00000463168.2:n.1441+69_1441+70delinsGT
ENST00000585317.2:n.3648+69_3648+70delinsGT
ENST00000676575.1:n.2961+69_2961+70delinsGT
ENST00000676581.1:c.*191+69_*191+70delinsGT	ENSP00000504407.1:n.*191+69_*191+70delinsGT
ENST00000676601.1:c.*456+69_*456+70delinsGT	ENSP00000504708.1:n.*456+69_*456+70delinsGT
ENST00000676785.1:c.1441+69_1441+70delinsGT	ENSP00000504794.1:n.1441+69_1441+70delinsGT
ENST00000676969.1:n.2213+69_2213+70delinsGT
ENST00000677726.1:c.*1056+69_*1056+70delinsGT	ENSP00000504260.1:n.*1056+69_*1056+70delinsGT
ENST00000678110.1:n.3138+69_3138+70delinsGT
ENST00000678757.1:c.*191+69_*191+70delinsGT	ENSP00000504731.1:n.*191+69_*191+70delinsGT
ENST00000678810.1:n.3272+69_3272+70delinsGT
ENST00000678814.1:c.*277+69_*277+70delinsGT	ENSP00000503045.1:n.*277+69_*277+70delinsGT
ENST00000678890.1:n.3465+69_3465+70delinsGT
ENST00000225792.9:c.1441+69_1441+70delinsGT	ENSP00000225792.5:n.1441+69_1441+70delinsGT
ENST00000450599.6:c.1204+69_1204+70delinsGT	ENSP00000403085.2:n.1204+69_1204+70delinsGT
ENST00000540698.6:c.*1053+69_*1053+70delinsGT	ENSP00000440276.2:n.*1053+69_*1053+70delinsGT
ENST00000578758.5:n.474+69_474+70delinsGT
ENST00000578804.5:c.1441+69_1441+70delinsGT	ENSP00000462885.1:n.1441+69_1441+70delinsGT
ENST00000580026.5:n.954+69_954+70delinsGT
ENST00000581230.5:n.2847+69_2847+70delinsGT
ENST00000581237.2:n.450+69_450+70delinsGT
ENST00000581693.5:c.*1158+69_*1158+70delinsGT	ENSP00000464566.1:n.*1158+69_*1158+70delinsGT
NM_004396.3:c.1441+69_1441+70delinsGT	NP_004387.1:n.1441+69_1441+70delinsGT
XM_005257111.1:c.1441+69_1441+70delinsGT	XP_005257168.1:n.1441+69_1441+70delinsGT
XM_006721738.1:c.1441+69_1441+70delinsGT	XP_006721801.1:n.1441+69_1441+70delinsGT
XM_011524456.1:c.1441+69_1441+70delinsGT	XP_011522758.1:n.1441+69_1441+70delinsGT
XM_011524457.1:c.1217-154_1217-153delinsGT	XP_011522759.1:n.1217-154_1217-153delinsGT
NM_001320595.1:c.1441+69_1441+70delinsGT	NP_001307524.1:n.1441+69_1441+70delinsGT
NM_001320596.2:c.1441+69_1441+70delinsGT	NP_001307525.1:n.1441+69_1441+70delinsGT
NM_001320597.1:c.1441+69_1441+70delinsGT	NP_001307526.1:n.1441+69_1441+70delinsGT
NM_004396.4:c.1441+69_1441+70delinsGT	NP_004387.1:n.1441+69_1441+70delinsGT
NM_001320595.2:c.1441+69_1441+70delinsGT	NP_001307524.1:n.1441+69_1441+70delinsGT
NM_001320597.2:c.1441+69_1441+70delinsGT	NP_001307526.1:n.1441+69_1441+70delinsGT
NM_004396.5:c.1441+69_1441+70delinsGT MANE Select	NP_004387.1:n.1441+69_1441+70delinsGT
NM_001320596.3:c.1441+69_1441+70delinsGT	NP_001307525.1:n.1441+69_1441+70delinsGT