Canonical Allele Identifier: CA400643000

Gene: DDX5

Linked Data

• MyVariant Identifiers: chr17:g.62496769G>C (hg19) ; chr17:g.64500651G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.64500651G>C , CM000679.2:g.64500651G>C	GRCh38
NC_000017.10:g.62496769G>C , CM000679.1:g.62496769G>C	GRCh37
NC_000017.9:g.59927231G>C	NCBI36
NG_013029.1:g.1416C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225792.10:c.1339C>G MANE Select	ENSP00000225792.5:p.Pro447Ala
ENST00000450599.7:c.1339C>G	ENSP00000403085.3:p.Pro447Ala
ENST00000577922.6:c.1339C>G	ENSP00000464337.2:p.Pro447Ala
ENST00000578491.2:n.2859C>G
ENST00000579461.2:n.3414C>G
ENST00000580026.6:n.2736C>G
ENST00000582326.2:n.4325C>G
ENST00000583212.2:c.1024C>G	ENSP00000463903.2:p.Pro342Ala
ENST00000585111.2:c.1339C>G	ENSP00000463168.2:p.Pro447Ala
ENST00000585317.2:n.3546C>G
ENST00000676575.1:n.2859C>G
ENST00000676581.1:c.*89C>G	ENSP00000504407.1:n.*89C>G
ENST00000676601.1:c.*354C>G	ENSP00000504708.1:n.*354C>G
ENST00000676785.1:c.1339C>G	ENSP00000504794.1:p.Pro447Ala
ENST00000676969.1:n.2111C>G
ENST00000677726.1:c.*954C>G	ENSP00000504260.1:n.*954C>G
ENST00000678110.1:n.3036C>G
ENST00000678757.1:c.*89C>G	ENSP00000504731.1:n.*89C>G
ENST00000678810.1:n.3170C>G
ENST00000678814.1:c.*175C>G	ENSP00000503045.1:n.*175C>G
ENST00000678890.1:n.3363C>G
ENST00000225792.9:c.1339C>G	ENSP00000225792.5:p.Pro447Ala
ENST00000450599.6:c.1102C>G	ENSP00000403085.2:p.Pro368Ala
ENST00000540698.6:c.*951C>G	ENSP00000440276.2:n.*951C>G
ENST00000578758.5:n.372C>G
ENST00000578804.5:c.1339C>G	ENSP00000462885.1:p.Pro447Ala
ENST00000580026.5:n.852C>G
ENST00000581230.5:n.2745C>G
ENST00000581237.2:n.348C>G
ENST00000581693.5:c.*1056C>G	ENSP00000464566.1:n.*1056C>G
NM_004396.3:c.1339C>G	NP_004387.1:p.Pro447Ala
XM_005257111.1:c.1339C>G	XP_005257168.1:p.Pro447Ala
XM_006721738.1:c.1339C>G	XP_006721801.1:p.Pro447Ala
XM_011524456.1:c.1339C>G	XP_011522758.1:p.Pro447Ala
XM_011524457.1:c.1217-325C>G	XP_011522759.1:n.1217-325C>G
NM_001320595.1:c.1339C>G	NP_001307524.1:p.Pro447Ala
NM_001320596.2:c.1339C>G	NP_001307525.1:p.Pro447Ala
NM_001320597.1:c.1339C>G	NP_001307526.1:p.Pro447Ala
NM_004396.4:c.1339C>G	NP_004387.1:p.Pro447Ala
NM_001320595.2:c.1339C>G	NP_001307524.1:p.Pro447Ala
NM_001320597.2:c.1339C>G	NP_001307526.1:p.Pro447Ala
NM_004396.5:c.1339C>G MANE Select	NP_004387.1:p.Pro447Ala
NM_001320596.3:c.1339C>G	NP_001307525.1:p.Pro447Ala