Canonical Allele Identifier: CA2166552673
Gene: HERC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28268167_28268168delinsGT , CM000677.2:g.28268167_28268168delinsGT GRCh38
NC_000015.9:g.28513313_28513314delinsGT , CM000677.1:g.28513313_28513314delinsGT GRCh37
NC_000015.8:g.26186908_26186909delinsGT NCBI36
NG_016355.1:g.58982_58983delinsAC

Transcript Alleles

HGVS Amino-acid change
ENST00000261609.13:c.1598+297_1598+298delinsAC MANE Select ENSP00000261609.8:n.1598+297_1598+298deli...
ENST00000261609.11:c.1598+297_1598+298delinsAC ENSP00000261609.7:n.1598+297_1598+298deli...
ENST00000564734.5:c.*1468+297_*1468+298delinsAC ENSP00000456237.1:n.*1468+297_*1468+298de...
NM_004667.5:c.1598+297_1598+298delinsAC NP_004658.3:n.1598+297_1598+298delinsAC
XM_005268276.3:c.1484+297_1484+298delinsAC XP_005268333.1:n.1484+297_1484+298delinsA...
XM_005268277.3:c.1484+297_1484+298delinsAC XP_005268334.1:n.1484+297_1484+298delinsA...
XM_006720726.2:c.1598+297_1598+298delinsAC XP_006720789.1:n.1598+297_1598+298delinsA...
XM_006720727.2:c.1340+297_1340+298delinsAC XP_006720790.1:n.1340+297_1340+298delinsA...
XM_011522131.1:c.1115+297_1115+298delinsAC XP_011520433.1:n.1115+297_1115+298delinsA...
XM_011522132.1:c.107+4047_107+4048delinsAC XP_011520434.1:n.107+4047_107+4048delinsA...
XM_011522133.1:c.322+24720_322+24721delinsAC XP_011520435.1:n.322+24720_322+24721delin...
XM_011522135.1:c.1598+297_1598+298delinsAC XP_011520437.1:n.1598+297_1598+298delinsA...
XM_011522136.1:c.1598+297_1598+298delinsAC XP_011520438.1:n.1598+297_1598+298delinsA...
XM_011522137.1:c.1598+297_1598+298delinsAC XP_011520439.1:n.1598+297_1598+298delinsA...
XR_931930.1:n.1727+297_1727+298delinsAC
XR_931931.1:n.1727+297_1727+298delinsAC
XM_005268276.5:c.1484+297_1484+298delinsAC XP_005268333.1:n.1484+297_1484+298delinsA...
XM_006720726.3:c.1598+297_1598+298delinsAC XP_006720789.1:n.1598+297_1598+298delinsA...
XM_006720727.3:c.1340+297_1340+298delinsAC XP_006720790.1:n.1340+297_1340+298delinsA...
XM_017022695.1:c.1484+297_1484+298delinsAC XP_016878184.1:n.1484+297_1484+298delinsA...
XM_017022696.1:c.1484+297_1484+298delinsAC XP_016878185.1:n.1484+297_1484+298delinsA...
XR_001751410.1:n.1728+297_1728+298delinsAC
XR_931930.2:n.1728+297_1728+298delinsAC
NM_004667.6:c.1598+297_1598+298delinsAC MANE Select NP_004658.3:n.1598+297_1598+298delinsAC