Canonical Allele Identifier: CA790697549
Gene: DDX60L HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000004.12:g.168409233C>G , CM000666.2:g.168409233C>G GRCh38
NC_000004.11:g.169330384C>G , CM000666.1:g.169330384C>G GRCh37
NC_000004.10:g.169566959C>G NCBI36
NG_051576.1:g.76282G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000682922.1:c.2980-2527G>C MANE Select ENSP00000507872.1:n.2980-2527G>C
ENST00000260184.11:c.2980-2527G>C ENSP00000260184.7:n.2980-2527G>C
ENST00000505863.1:c.2068-2527G>C ENSP00000421026.1:n.2068-2527G>C
ENST00000505890.5:c.2980-2527G>C ENSP00000422202.1:n.2980-2527G>C
ENST00000511577.5:c.2980-2527G>C ENSP00000422423.1:n.2980-2527G>C
NM_001012967.2:c.2980-2527G>C NP_001012985.2:n.2980-2527G>C
NM_001291510.1:c.2980-2527G>C NP_001278439.1:n.2980-2527G>C
XM_005263341.3:c.2980-2527G>C XP_005263398.2:n.2980-2527G>C
XM_005263342.2:c.2980-2527G>C XP_005263399.2:n.2980-2527G>C
XM_005263343.2:c.2980-2527G>C XP_005263400.2:n.2980-2527G>C
XM_005263345.3:c.2980-2527G>C XP_005263402.2:n.2980-2527G>C
XM_006714408.2:c.2980-2527G>C XP_006714471.1:n.2980-2527G>C
XM_011532402.1:c.2980-2527G>C XP_011530704.1:n.2980-2527G>C
XM_011532403.1:c.2980-2527G>C XP_011530705.1:n.2980-2527G>C
XM_011532404.1:c.2884-2527G>C XP_011530706.1:n.2884-2527G>C
XM_011532405.1:c.2884-2527G>C XP_011530707.1:n.2884-2527G>C
XM_011532406.1:c.2980-2527G>C XP_011530708.1:n.2980-2527G>C
XM_011532407.1:c.2155-2527G>C XP_011530709.1:n.2155-2527G>C
XM_011532408.1:c.1138-2527G>C XP_011530710.1:n.1138-2527G>C
XM_011532409.1:c.1138-2527G>C XP_011530711.1:n.1138-2527G>C
XR_938792.1:n.3228-2527G>C
NM_001345927.1:c.2980-2527G>C NP_001332856.1:n.2980-2527G>C
XM_005263341.4:c.2980-2527G>C XP_005263398.2:n.2980-2527G>C
XM_005263345.4:c.2980-2527G>C XP_005263402.2:n.2980-2527G>C
XM_011532402.2:c.2980-2527G>C XP_011530704.1:n.2980-2527G>C
XM_011532403.2:c.2980-2527G>C XP_011530705.1:n.2980-2527G>C
XM_011532409.3:c.1138-2527G>C XP_011530711.1:n.1138-2527G>C
XM_017008829.1:c.2884-2527G>C XP_016864318.1:n.2884-2527G>C
XM_017008830.1:c.2980-2527G>C XP_016864319.1:n.2980-2527G>C
XM_017008831.1:c.1138-2527G>C XP_016864320.1:n.1138-2527G>C
NM_001291510.2:c.2980-2527G>C NP_001278439.1:n.2980-2527G>C
NM_001345927.2:c.2980-2527G>C NP_001332856.1:n.2980-2527G>C
NM_001012967.3:c.2980-2527G>C MANE Select NP_001012985.2:n.2980-2527G>C
NM_001378072.1:c.2980-2527G>C NP_001365001.1:n.2980-2527G>C