Canonical Allele Identifier: CA2576358365

Gene: DDX5

Linked Data

• gnomAD v4: 17-64500502-A-G

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.64500502A>G , CM000679.2:g.64500502A>G	GRCh38
NC_000017.10:g.62496620A>G , CM000679.1:g.62496620A>G	GRCh37
NC_000017.9:g.59927082A>G	NCBI36
NG_013029.1:g.1565T>C

Transcript Alleles

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