Canonical Allele Identifier: CA501460192

Gene: DDX5

Linked Data

• MyVariant Identifiers: chr17:g.62496767A>T (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.64500649A>T , CM000679.2:g.64500649A>T	GRCh38
NC_000017.10:g.62496767A>T , CM000679.1:g.62496767A>T	GRCh37
NC_000017.9:g.59927229A>T	NCBI36
NG_013029.1:g.1418T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225792.10:c.1341T>A MANE Select	ENSP00000225792.5:p.Pro447=
ENST00000450599.7:c.1341T>A	ENSP00000403085.3:p.Pro447=
ENST00000577922.6:c.1341T>A	ENSP00000464337.2:p.Pro447=
ENST00000578491.2:n.2861T>A
ENST00000579461.2:n.3416T>A
ENST00000580026.6:n.2738T>A
ENST00000582326.2:n.4327T>A
ENST00000583212.2:c.1026T>A	ENSP00000463903.2:p.Pro342=
ENST00000585111.2:c.1341T>A	ENSP00000463168.2:p.Pro447=
ENST00000585317.2:n.3548T>A
ENST00000676575.1:n.2861T>A
ENST00000676581.1:c.*91T>A	ENSP00000504407.1:n.*91T>A
ENST00000676601.1:c.*356T>A	ENSP00000504708.1:n.*356T>A
ENST00000676785.1:c.1341T>A	ENSP00000504794.1:p.Pro447=
ENST00000676969.1:n.2113T>A
ENST00000677726.1:c.*956T>A	ENSP00000504260.1:n.*956T>A
ENST00000678110.1:n.3038T>A
ENST00000678757.1:c.*91T>A	ENSP00000504731.1:n.*91T>A
ENST00000678810.1:n.3172T>A
ENST00000678814.1:c.*177T>A	ENSP00000503045.1:n.*177T>A
ENST00000678890.1:n.3365T>A
ENST00000225792.9:c.1341T>A	ENSP00000225792.5:p.Pro447=
ENST00000450599.6:c.1104T>A	ENSP00000403085.2:p.Pro368=
ENST00000540698.6:c.*953T>A	ENSP00000440276.2:n.*953T>A
ENST00000578758.5:n.374T>A
ENST00000578804.5:c.1341T>A	ENSP00000462885.1:p.Pro447=
ENST00000580026.5:n.854T>A
ENST00000581230.5:n.2747T>A
ENST00000581237.2:n.350T>A
ENST00000581693.5:c.*1058T>A	ENSP00000464566.1:n.*1058T>A
NM_004396.3:c.1341T>A	NP_004387.1:p.Pro447=
XM_005257111.1:c.1341T>A	XP_005257168.1:p.Pro447=
XM_006721738.1:c.1341T>A	XP_006721801.1:p.Pro447=
XM_011524456.1:c.1341T>A	XP_011522758.1:p.Pro447=
XM_011524457.1:c.1217-323T>A	XP_011522759.1:n.1217-323T>A
NM_001320595.1:c.1341T>A	NP_001307524.1:p.Pro447=
NM_001320596.2:c.1341T>A	NP_001307525.1:p.Pro447=
NM_001320597.1:c.1341T>A	NP_001307526.1:p.Pro447=
NM_004396.4:c.1341T>A	NP_004387.1:p.Pro447=
NM_001320595.2:c.1341T>A	NP_001307524.1:p.Pro447=
NM_001320597.2:c.1341T>A	NP_001307526.1:p.Pro447=
NM_004396.5:c.1341T>A MANE Select	NP_004387.1:p.Pro447=
NM_001320596.3:c.1341T>A	NP_001307525.1:p.Pro447=