Canonical Allele Identifier: CA2166566587
Gene: HERC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28285129_28285130delinsCT , CM000677.2:g.28285129_28285130delinsCT GRCh38
NC_000015.9:g.28530275_28530276delinsCT , CM000677.1:g.28530275_28530276delinsCT GRCh37
NC_000015.8:g.26203870_26203871delinsCT NCBI36
NG_016355.1:g.42020_42021delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000261609.13:c.323-4843_323-4842delinsAG MANE Select ENSP00000261609.8:n.323-4843_323-4842deli...
ENST00000261609.11:c.323-4843_323-4842delinsAG ENSP00000261609.7:n.323-4843_323-4842deli...
ENST00000564383.1:n.218-4843_218-4842delinsAG
ENST00000564734.5:c.*193-4843_*193-4842delinsAG ENSP00000456237.1:n.*193-4843_*193-4842de...
NM_004667.5:c.323-4843_323-4842delinsAG NP_004658.3:n.323-4843_323-4842delinsAG
XM_005268276.3:c.209-4843_209-4842delinsAG XP_005268333.1:n.209-4843_209-4842delinsA...
XM_005268277.3:c.209-4843_209-4842delinsAG XP_005268334.1:n.209-4843_209-4842delinsA...
XM_006720726.2:c.323-4843_323-4842delinsAG XP_006720789.1:n.323-4843_323-4842delinsA...
XM_006720727.2:c.323-4843_323-4842delinsAG XP_006720790.1:n.323-4843_323-4842delinsA...
XM_011522133.1:c.322+7758_322+7759delinsAG XP_011520435.1:n.322+7758_322+7759delinsA...
XM_011522135.1:c.323-4843_323-4842delinsAG XP_011520437.1:n.323-4843_323-4842delinsA...
XM_011522136.1:c.323-4843_323-4842delinsAG XP_011520438.1:n.323-4843_323-4842delinsA...
XM_011522137.1:c.323-4843_323-4842delinsAG XP_011520439.1:n.323-4843_323-4842delinsA...
XR_931930.1:n.452-4843_452-4842delinsAG
XR_931931.1:n.452-4843_452-4842delinsAG
XM_005268276.5:c.209-4843_209-4842delinsAG XP_005268333.1:n.209-4843_209-4842delinsA...
XM_006720726.3:c.323-4843_323-4842delinsAG XP_006720789.1:n.323-4843_323-4842delinsA...
XM_006720727.3:c.323-4843_323-4842delinsAG XP_006720790.1:n.323-4843_323-4842delinsA...
XM_017022695.1:c.209-4843_209-4842delinsAG XP_016878184.1:n.209-4843_209-4842delinsA...
XM_017022696.1:c.209-4843_209-4842delinsAG XP_016878185.1:n.209-4843_209-4842delinsA...
XR_001751410.1:n.453-4843_453-4842delinsAG
XR_931930.2:n.453-4843_453-4842delinsAG
NM_004667.6:c.323-4843_323-4842delinsAG MANE Select NP_004658.3:n.323-4843_323-4842delinsAG