Canonical Allele Identifier: CA968036288
Gene: HERC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28284949_28284950insAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAA , CM000677.2:g.28284949_28284950insAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAA GRCh38
NC_000015.9:g.28530095_28530096insAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAA , CM000677.1:g.28530095_28530096insAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAA GRCh37
NC_000015.8:g.26203690_26203691insAAAAAAAAAACAAAAAAAAAAAAAAAAAAAAAAA NCBI36
NG_016355.1:g.42223_42224insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS Amino-acid Change
ENST00000261609.13:c.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select ENSP00000261609.8:n.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTT...
ENST00000261609.11:c.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000261609.7:n.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTT...
ENST00000564383.1:n.218-4640_218-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000564734.5:c.*193-4640_*193-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT ENSP00000456237.1:n.*193-4640_*193-4639insGTTTTTTTTTTTTTTTTTT...
NM_004667.5:c.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT NP_004658.3:n.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_005268276.3:c.209-4640_209-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_005268333.1:n.209-4640_209-4639insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_005268277.3:c.209-4640_209-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_005268334.1:n.209-4640_209-4639insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_006720726.2:c.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_006720789.1:n.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_006720727.2:c.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_006720790.1:n.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_011522133.1:c.322+7961_322+7962insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011520435.1:n.322+7961_322+7962insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_011522135.1:c.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011520437.1:n.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_011522136.1:c.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011520438.1:n.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_011522137.1:c.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_011520439.1:n.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTTTTT...
XR_931930.1:n.452-4640_452-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XR_931931.1:n.452-4640_452-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XM_005268276.5:c.209-4640_209-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_005268333.1:n.209-4640_209-4639insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_006720726.3:c.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_006720789.1:n.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_006720727.3:c.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_006720790.1:n.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_017022695.1:c.209-4640_209-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_016878184.1:n.209-4640_209-4639insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_017022696.1:c.209-4640_209-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT XP_016878185.1:n.209-4640_209-4639insGTTTTTTTTTTTTTTTTTTTTTTT...
XR_001751410.1:n.453-4640_453-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XR_931930.2:n.453-4640_453-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_004667.6:c.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select NP_004658.3:n.323-4640_323-4639insGTTTTTTTTTTTTTTTTTTTTTTTTTT...