Canonical Allele Identifier: CA2270407658

Gene: DDX5

Genomic Alleles

HGVS	Genome Assembly
NC_000017.11:g.64500552A= , CM000679.2:g.64500552A=	GRCh38
NC_000017.10:g.62496670A= , CM000679.1:g.62496670A=	GRCh37
NC_000017.9:g.59927132A=	NCBI36
NG_013029.1:g.1515T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000225792.10:c.1438T= MANE Select	ENSP00000225792.5:p.Ser480=
ENST00000450599.7:c.1438T=	ENSP00000403085.3:p.Ser480=
ENST00000577922.6:c.1438T=	ENSP00000464337.2:p.Ser480=
ENST00000578491.2:n.2958T=
ENST00000579461.2:n.3513T=
ENST00000580026.6:n.2835T=
ENST00000582326.2:n.4424T=
ENST00000583212.2:c.1123T=	ENSP00000463903.2:p.Ser375=
ENST00000585111.2:c.1438T=	ENSP00000463168.2:p.Ser480=
ENST00000585317.2:n.3645T=
ENST00000676575.1:n.2958T=
ENST00000676581.1:c.*188T=	ENSP00000504407.1:n.*188T=
ENST00000676601.1:c.*453T=	ENSP00000504708.1:n.*453T=
ENST00000676785.1:c.1438T=	ENSP00000504794.1:p.Ser480=
ENST00000676969.1:n.2210T=
ENST00000677726.1:c.*1053T=	ENSP00000504260.1:n.*1053T=
ENST00000678110.1:n.3135T=
ENST00000678757.1:c.*188T=	ENSP00000504731.1:n.*188T=
ENST00000678810.1:n.3269T=
ENST00000678814.1:c.*274T=	ENSP00000503045.1:n.*274T=
ENST00000678890.1:n.3462T=
ENST00000225792.9:c.1438T=	ENSP00000225792.5:p.Ser480=
ENST00000450599.6:c.1201T=	ENSP00000403085.2:p.Ser401=
ENST00000540698.6:c.*1050T=	ENSP00000440276.2:n.*1050T=
ENST00000578758.5:n.471T=
ENST00000578804.5:c.1438T=	ENSP00000462885.1:p.Ser480=
ENST00000580026.5:n.951T=
ENST00000581230.5:n.2844T=
ENST00000581237.2:n.447T=
ENST00000581693.5:c.*1155T=	ENSP00000464566.1:n.*1155T=
NM_004396.3:c.1438T=	NP_004387.1:p.Ser480=
XM_005257111.1:c.1438T=	XP_005257168.1:p.Ser480=
XM_006721738.1:c.1438T=	XP_006721801.1:p.Ser480=
XM_011524456.1:c.1438T=	XP_011522758.1:p.Ser480=
XM_011524457.1:c.1217-226T=	XP_011522759.1:n.1217-226T=
NM_001320595.1:c.1438T=	NP_001307524.1:p.Ser480=
NM_001320596.2:c.1438T=	NP_001307525.1:p.Ser480=
NM_001320597.1:c.1438T=	NP_001307526.1:p.Ser480=
NM_004396.4:c.1438T=	NP_004387.1:p.Ser480=
NM_001320595.2:c.1438T=	NP_001307524.1:p.Ser480=
NM_001320597.2:c.1438T=	NP_001307526.1:p.Ser480=
NM_004396.5:c.1438T= MANE Select	NP_004387.1:p.Ser480=
NM_001320596.3:c.1438T=	NP_001307525.1:p.Ser480=