Canonical Allele Identifier: CA400642906

Gene: DDX5

Linked Data

• MyVariant Identifiers: chr17:g.62496727G>C (hg19) ; chr17:g.64500609G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.64500609G>C , CM000679.2:g.64500609G>C	GRCh38
NC_000017.10:g.62496727G>C , CM000679.1:g.62496727G>C	GRCh37
NC_000017.9:g.59927189G>C	NCBI36
NG_013029.1:g.1458C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225792.10:c.1381C>G MANE Select	ENSP00000225792.5:p.Arg461Gly
ENST00000450599.7:c.1381C>G	ENSP00000403085.3:p.Arg461Gly
ENST00000577922.6:c.1381C>G	ENSP00000464337.2:p.Arg461Gly
ENST00000578491.2:n.2901C>G
ENST00000579461.2:n.3456C>G
ENST00000580026.6:n.2778C>G
ENST00000582326.2:n.4367C>G
ENST00000583212.2:c.1066C>G	ENSP00000463903.2:p.Arg356Gly
ENST00000585111.2:c.1381C>G	ENSP00000463168.2:p.Arg461Gly
ENST00000585317.2:n.3588C>G
ENST00000676575.1:n.2901C>G
ENST00000676581.1:c.*131C>G	ENSP00000504407.1:n.*131C>G
ENST00000676601.1:c.*396C>G	ENSP00000504708.1:n.*396C>G
ENST00000676785.1:c.1381C>G	ENSP00000504794.1:p.Arg461Gly
ENST00000676969.1:n.2153C>G
ENST00000677726.1:c.*996C>G	ENSP00000504260.1:n.*996C>G
ENST00000678110.1:n.3078C>G
ENST00000678757.1:c.*131C>G	ENSP00000504731.1:n.*131C>G
ENST00000678810.1:n.3212C>G
ENST00000678814.1:c.*217C>G	ENSP00000503045.1:n.*217C>G
ENST00000678890.1:n.3405C>G
ENST00000225792.9:c.1381C>G	ENSP00000225792.5:p.Arg461Gly
ENST00000450599.6:c.1144C>G	ENSP00000403085.2:p.Arg382Gly
ENST00000540698.6:c.*993C>G	ENSP00000440276.2:n.*993C>G
ENST00000578758.5:n.414C>G
ENST00000578804.5:c.1381C>G	ENSP00000462885.1:p.Arg461Gly
ENST00000580026.5:n.894C>G
ENST00000581230.5:n.2787C>G
ENST00000581237.2:n.390C>G
ENST00000581693.5:c.*1098C>G	ENSP00000464566.1:n.*1098C>G
NM_004396.3:c.1381C>G	NP_004387.1:p.Arg461Gly
XM_005257111.1:c.1381C>G	XP_005257168.1:p.Arg461Gly
XM_006721738.1:c.1381C>G	XP_006721801.1:p.Arg461Gly
XM_011524456.1:c.1381C>G	XP_011522758.1:p.Arg461Gly
XM_011524457.1:c.1217-283C>G	XP_011522759.1:n.1217-283C>G
NM_001320595.1:c.1381C>G	NP_001307524.1:p.Arg461Gly
NM_001320596.2:c.1381C>G	NP_001307525.1:p.Arg461Gly
NM_001320597.1:c.1381C>G	NP_001307526.1:p.Arg461Gly
NM_004396.4:c.1381C>G	NP_004387.1:p.Arg461Gly
NM_001320595.2:c.1381C>G	NP_001307524.1:p.Arg461Gly
NM_001320597.2:c.1381C>G	NP_001307526.1:p.Arg461Gly
NM_004396.5:c.1381C>G MANE Select	NP_004387.1:p.Arg461Gly
NM_001320596.3:c.1381C>G	NP_001307525.1:p.Arg461Gly