Canonical Allele Identifier: CA2270407625

Gene: DDX5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.64500499_64500502delinsGACA , CM000679.2:g.64500499_64500502delinsGACA	GRCh38
NC_000017.10:g.62496617_62496620delinsGACA , CM000679.1:g.62496617_62496620delinsGACA	GRCh37
NC_000017.9:g.59927079_59927082delinsGACA	NCBI36
NG_013029.1:g.1565_1568delinsTGTC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225792.10:c.1441+47_1441+50delinsTGTC MANE Select	ENSP00000225792.5:n.1441+47_1441+50delinsTGTC
ENST00000450599.7:c.1441+47_1441+50delinsTGTC	ENSP00000403085.3:n.1441+47_1441+50delinsTGTC
ENST00000577922.6:c.1441+47_1441+50delinsTGTC	ENSP00000464337.2:n.1441+47_1441+50delinsTGTC
ENST00000578491.2:n.3008_3011delinsTGTC
ENST00000579461.2:n.3563_3566delinsTGTC
ENST00000580026.6:n.2838+47_2838+50delinsTGTC
ENST00000582326.2:n.4474_4477delinsTGTC
ENST00000583212.2:c.1126+47_1126+50delinsTGTC	ENSP00000463903.2:n.1126+47_1126+50delinsTGTC
ENST00000585111.2:c.1441+47_1441+50delinsTGTC	ENSP00000463168.2:n.1441+47_1441+50delinsTGTC
ENST00000585317.2:n.3648+47_3648+50delinsTGTC
ENST00000676575.1:n.2961+47_2961+50delinsTGTC
ENST00000676581.1:c.*191+47_*191+50delinsTGTC	ENSP00000504407.1:n.*191+47_*191+50delinsTGTC
ENST00000676601.1:c.*456+47_*456+50delinsTGTC	ENSP00000504708.1:n.*456+47_*456+50delinsTGTC
ENST00000676785.1:c.1441+47_1441+50delinsTGTC	ENSP00000504794.1:n.1441+47_1441+50delinsTGTC
ENST00000676969.1:n.2213+47_2213+50delinsTGTC
ENST00000677726.1:c.*1056+47_*1056+50delinsTGTC	ENSP00000504260.1:n.*1056+47_*1056+50delinsTGTC
ENST00000678110.1:n.3138+47_3138+50delinsTGTC
ENST00000678757.1:c.*191+47_*191+50delinsTGTC	ENSP00000504731.1:n.*191+47_*191+50delinsTGTC
ENST00000678810.1:n.3272+47_3272+50delinsTGTC
ENST00000678814.1:c.*277+47_*277+50delinsTGTC	ENSP00000503045.1:n.*277+47_*277+50delinsTGTC
ENST00000678890.1:n.3465+47_3465+50delinsTGTC
ENST00000225792.9:c.1441+47_1441+50delinsTGTC	ENSP00000225792.5:n.1441+47_1441+50delinsTGTC
ENST00000450599.6:c.1204+47_1204+50delinsTGTC	ENSP00000403085.2:n.1204+47_1204+50delinsTGTC
ENST00000540698.6:c.*1053+47_*1053+50delinsTGTC	ENSP00000440276.2:n.*1053+47_*1053+50delinsTGTC
ENST00000578758.5:n.474+47_474+50delinsTGTC
ENST00000578804.5:c.1441+47_1441+50delinsTGTC	ENSP00000462885.1:n.1441+47_1441+50delinsTGTC
ENST00000580026.5:n.954+47_954+50delinsTGTC
ENST00000581230.5:n.2847+47_2847+50delinsTGTC
ENST00000581237.2:n.450+47_450+50delinsTGTC
ENST00000581693.5:c.*1158+47_*1158+50delinsTGTC	ENSP00000464566.1:n.*1158+47_*1158+50delinsTGTC
NM_004396.3:c.1441+47_1441+50delinsTGTC	NP_004387.1:n.1441+47_1441+50delinsTGTC
XM_005257111.1:c.1441+47_1441+50delinsTGTC	XP_005257168.1:n.1441+47_1441+50delinsTGTC
XM_006721738.1:c.1441+47_1441+50delinsTGTC	XP_006721801.1:n.1441+47_1441+50delinsTGTC
XM_011524456.1:c.1441+47_1441+50delinsTGTC	XP_011522758.1:n.1441+47_1441+50delinsTGTC
XM_011524457.1:c.1217-176_1217-173delinsTGTC	XP_011522759.1:n.1217-176_1217-173delinsTGTC
NM_001320595.1:c.1441+47_1441+50delinsTGTC	NP_001307524.1:n.1441+47_1441+50delinsTGTC
NM_001320596.2:c.1441+47_1441+50delinsTGTC	NP_001307525.1:n.1441+47_1441+50delinsTGTC
NM_001320597.1:c.1441+47_1441+50delinsTGTC	NP_001307526.1:n.1441+47_1441+50delinsTGTC
NM_004396.4:c.1441+47_1441+50delinsTGTC	NP_004387.1:n.1441+47_1441+50delinsTGTC
NM_001320595.2:c.1441+47_1441+50delinsTGTC	NP_001307524.1:n.1441+47_1441+50delinsTGTC
NM_001320597.2:c.1441+47_1441+50delinsTGTC	NP_001307526.1:n.1441+47_1441+50delinsTGTC
NM_004396.5:c.1441+47_1441+50delinsTGTC MANE Select	NP_004387.1:n.1441+47_1441+50delinsTGTC
NM_001320596.3:c.1441+47_1441+50delinsTGTC	NP_001307525.1:n.1441+47_1441+50delinsTGTC