Canonical Allele Identifier: CA2830535206
Gene: DDX60 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168255604_168255605insTTGT , CM000666.2:g.168255604_168255605insTTGT GRCh38
NC_000004.11:g.169176755_169176756insTTGT , CM000666.1:g.169176755_169176756insTTGT GRCh37
NC_000004.10:g.169413330_169413331insTTGT NCBI36
NG_054636.1:g.68203_68204insACAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000393743.8:c.3557+106_3557+107insACAA MANE Select ENSP00000377344.3:n.3557+106_3557+107insACAA
ENST00000679510.1:c.3557+106_3557+107insACAA ENSP00000506501.1:n.3557+106_3557+107insACAA
ENST00000680771.1:c.3557+106_3557+107insACAA ENSP00000505292.1:n.3557+106_3557+107insACAA
ENST00000680917.1:c.*3007_*3008insACAA ENSP00000505790.1:n.*3007_*3008insACAA
ENST00000393743.7:c.3557+106_3557+107insACAA ENSP00000377344.3:n.3557+106_3557+107insACAA
ENST00000505393.1:n.662+106_662+107insACAA
NM_017631.5:c.3557+106_3557+107insACAA NP_060101.3:n.3557+106_3557+107insACAA
XM_011532103.1:c.3557+106_3557+107insACAA XP_011530405.1:n.3557+106_3557+107insACAA
XM_011532103.3:c.3557+106_3557+107insACAA XP_011530405.1:n.3557+106_3557+107insACAA
XM_024454132.1:c.3557+106_3557+107insACAA XP_024309900.1:n.3557+106_3557+107insACAA
XM_024454133.1:c.3557+106_3557+107insACAA XP_024309901.1:n.3557+106_3557+107insACAA
NM_017631.6:c.3557+106_3557+107insACAA MANE Select NP_060101.3:n.3557+106_3557+107insACAA