Canonical Allele Identifier: CA968036348
Gene: HERC2 HGNC NCBI

Linked Data

dbSNP Id: rs2076117677

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28284950_28284951del , CM000677.2:g.28284950_28284951del GRCh38
NC_000015.9:g.28530096_28530097del , CM000677.1:g.28530096_28530097del GRCh37
NC_000015.8:g.26203691_26203692del NCBI36
NG_016355.1:g.42200_42201del

Transcript Alleles

HGVS Amino-acid change
ENST00000261609.13:c.323-4663_323-4662del MANE Select ENSP00000261609.8:n.323-4663_323-4662del
ENST00000261609.11:c.323-4663_323-4662del ENSP00000261609.7:n.323-4663_323-4662del
ENST00000564383.1:n.218-4663_218-4662del
ENST00000564734.5:c.*193-4663_*193-4662del ENSP00000456237.1:n.*193-4663_*193-4662de...
NM_004667.5:c.323-4663_323-4662del NP_004658.3:n.323-4663_323-4662del
XM_005268276.3:c.209-4663_209-4662del XP_005268333.1:n.209-4663_209-4662del
XM_005268277.3:c.209-4663_209-4662del XP_005268334.1:n.209-4663_209-4662del
XM_006720726.2:c.323-4663_323-4662del XP_006720789.1:n.323-4663_323-4662del
XM_006720727.2:c.323-4663_323-4662del XP_006720790.1:n.323-4663_323-4662del
XM_011522133.1:c.322+7938_322+7939del XP_011520435.1:n.322+7938_322+7939del
XM_011522135.1:c.323-4663_323-4662del XP_011520437.1:n.323-4663_323-4662del
XM_011522136.1:c.323-4663_323-4662del XP_011520438.1:n.323-4663_323-4662del
XM_011522137.1:c.323-4663_323-4662del XP_011520439.1:n.323-4663_323-4662del
XR_931930.1:n.452-4663_452-4662del
XR_931931.1:n.452-4663_452-4662del
XM_005268276.5:c.209-4663_209-4662del XP_005268333.1:n.209-4663_209-4662del
XM_006720726.3:c.323-4663_323-4662del XP_006720789.1:n.323-4663_323-4662del
XM_006720727.3:c.323-4663_323-4662del XP_006720790.1:n.323-4663_323-4662del
XM_017022695.1:c.209-4663_209-4662del XP_016878184.1:n.209-4663_209-4662del
XM_017022696.1:c.209-4663_209-4662del XP_016878185.1:n.209-4663_209-4662del
XR_001751410.1:n.453-4663_453-4662del
XR_931930.2:n.453-4663_453-4662del
NM_004667.6:c.323-4663_323-4662del MANE Select NP_004658.3:n.323-4663_323-4662del