Canonical Allele Identifier: CA968036367
Gene: HERC2 HGNC NCBI

Linked Data

dbSNP Id: rs2141083030

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28284953_28284954dup , CM000677.2:g.28284953_28284954dup GRCh38
NC_000015.9:g.28530099_28530100dup , CM000677.1:g.28530099_28530100dup GRCh37
NC_000015.8:g.26203694_26203695dup NCBI36
NG_016355.1:g.42196_42197dup

Transcript Alleles

HGVS Amino-acid change
ENST00000261609.13:c.323-4667_323-4666dup MANE Select ENSP00000261609.8:n.323-4667_323-4666dup
ENST00000261609.11:c.323-4667_323-4666dup ENSP00000261609.7:n.323-4667_323-4666dup
ENST00000564383.1:n.218-4667_218-4666dup
ENST00000564734.5:c.*193-4667_*193-4666dup ENSP00000456237.1:n.*193-4667_*193-4666du...
NM_004667.5:c.323-4667_323-4666dup NP_004658.3:n.323-4667_323-4666dup
XM_005268276.3:c.209-4667_209-4666dup XP_005268333.1:n.209-4667_209-4666dup
XM_005268277.3:c.209-4667_209-4666dup XP_005268334.1:n.209-4667_209-4666dup
XM_006720726.2:c.323-4667_323-4666dup XP_006720789.1:n.323-4667_323-4666dup
XM_006720727.2:c.323-4667_323-4666dup XP_006720790.1:n.323-4667_323-4666dup
XM_011522133.1:c.322+7934_322+7935dup XP_011520435.1:n.322+7934_322+7935dup
XM_011522135.1:c.323-4667_323-4666dup XP_011520437.1:n.323-4667_323-4666dup
XM_011522136.1:c.323-4667_323-4666dup XP_011520438.1:n.323-4667_323-4666dup
XM_011522137.1:c.323-4667_323-4666dup XP_011520439.1:n.323-4667_323-4666dup
XR_931930.1:n.452-4667_452-4666dup
XR_931931.1:n.452-4667_452-4666dup
XM_005268276.5:c.209-4667_209-4666dup XP_005268333.1:n.209-4667_209-4666dup
XM_006720726.3:c.323-4667_323-4666dup XP_006720789.1:n.323-4667_323-4666dup
XM_006720727.3:c.323-4667_323-4666dup XP_006720790.1:n.323-4667_323-4666dup
XM_017022695.1:c.209-4667_209-4666dup XP_016878184.1:n.209-4667_209-4666dup
XM_017022696.1:c.209-4667_209-4666dup XP_016878185.1:n.209-4667_209-4666dup
XR_001751410.1:n.453-4667_453-4666dup
XR_931930.2:n.453-4667_453-4666dup
NM_004667.6:c.323-4667_323-4666dup MANE Select NP_004658.3:n.323-4667_323-4666dup