Canonical Allele Identifier: CA132895525

Gene: DDX41

Genomic Alleles

HGVS	Genome Assembly
NC_000005.10:g.177516431dup , CM000667.2:g.177516431dup	GRCh38
NC_000005.9:g.176943432dup , CM000667.1:g.176943432dup	GRCh37
NC_000005.8:g.176876038dup	NCBI36
NG_046846.1:g.5896dup
NG_046846.2:g.5531dup

Transcript Alleles

HGVS	Amino-acid Change
NM_016222.4:c.155dup MANE Select	NP_057306.2:p.Arg53AlafsTer16
ENST00000330503.12:c.155dup MANE Select	ENSP00000330349.8:p.Arg53AlafsTer16
NM_001321732.1:c.-224dup	NP_001308661.1:n.-224dup
NM_001321732.2:c.-224dup	NP_001308661.1:n.-224dup
NM_001321830.1:c.-224dup	NP_001308759.1:n.-224dup
NM_001321830.2:c.-224dup	NP_001308759.1:n.-224dup
NM_016222.2:c.155dup	NP_057306.2:p.Arg53AlafsTer16
NM_016222.3:c.155dup	NP_057306.2:p.Arg53AlafsTer16
ENST00000330503.11:c.209dup	ENSP00000330349.7:p.Arg71AlafsTer16
ENST00000503078.5:n.448dup
ENST00000505081.5:n.160dup
ENST00000506965.5:n.160dup
ENST00000507955.5:c.155dup	ENSP00000422753.1:p.Arg53AlafsTer16
ENST00000507955.6:c.155dup	ENSP00000422753.2:p.Arg53AlafsTer16
ENST00000509576.5:c.155dup	ENSP00000426330.1:p.Arg53AlafsTer16
ENST00000510171.3:c.*74dup	ENSP00000427082.1:n.*74dup
ENST00000512431.5:n.145dup
ENST00000515562.1:n.188dup
ENST00000629036.2:c.155dup	ENSP00000486367.1:p.Arg53AlafsTer16
ENST00000650742.1:n.172dup
ENST00000652618.1:n.208dup
ENST00000652623.1:n.227dup
XM_006714870.1:c.-224dup	XP_006714933.1:n.-224dup
XM_024446109.1:c.-332dup	XP_024301877.1:n.-332dup