Canonical Allele Identifier: CA968034679
Gene: HERC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28284917_28284918insT , CM000677.2:g.28284917_28284918insT GRCh38
NC_000015.9:g.28530063_28530064insT , CM000677.1:g.28530063_28530064insT GRCh37
NC_000015.8:g.26203658_26203659insT NCBI36
NG_016355.1:g.42232_42233insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000261609.13:c.323-4631_323-4630insA MANE Select ENSP00000261609.8:n.323-4631_323-4630insA
ENST00000261609.11:c.323-4631_323-4630insA ENSP00000261609.7:n.323-4631_323-4630insA
ENST00000564383.1:n.218-4631_218-4630insA
ENST00000564734.5:c.*193-4631_*193-4630insA ENSP00000456237.1:n.*193-4631_*193-4630insA
NM_004667.5:c.323-4631_323-4630insA NP_004658.3:n.323-4631_323-4630insA
XM_005268276.3:c.209-4631_209-4630insA XP_005268333.1:n.209-4631_209-4630insA
XM_005268277.3:c.209-4631_209-4630insA XP_005268334.1:n.209-4631_209-4630insA
XM_006720726.2:c.323-4631_323-4630insA XP_006720789.1:n.323-4631_323-4630insA
XM_006720727.2:c.323-4631_323-4630insA XP_006720790.1:n.323-4631_323-4630insA
XM_011522133.1:c.322+7970_322+7971insA XP_011520435.1:n.322+7970_322+7971insA
XM_011522135.1:c.323-4631_323-4630insA XP_011520437.1:n.323-4631_323-4630insA
XM_011522136.1:c.323-4631_323-4630insA XP_011520438.1:n.323-4631_323-4630insA
XM_011522137.1:c.323-4631_323-4630insA XP_011520439.1:n.323-4631_323-4630insA
XR_931930.1:n.452-4631_452-4630insA
XR_931931.1:n.452-4631_452-4630insA
XM_005268276.5:c.209-4631_209-4630insA XP_005268333.1:n.209-4631_209-4630insA
XM_006720726.3:c.323-4631_323-4630insA XP_006720789.1:n.323-4631_323-4630insA
XM_006720727.3:c.323-4631_323-4630insA XP_006720790.1:n.323-4631_323-4630insA
XM_017022695.1:c.209-4631_209-4630insA XP_016878184.1:n.209-4631_209-4630insA
XM_017022696.1:c.209-4631_209-4630insA XP_016878185.1:n.209-4631_209-4630insA
XR_001751410.1:n.453-4631_453-4630insA
XR_931930.2:n.453-4631_453-4630insA
NM_004667.6:c.323-4631_323-4630insA MANE Select NP_004658.3:n.323-4631_323-4630insA