Canonical Allele Identifier: CA2166473228
Gene: HERC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28111727_28111735delinsGCTCAGGCT , CM000677.2:g.28111727_28111735delinsGCTCAGGCT GRCh38
NC_000015.9:g.28356873_28356881delinsGCTCAGGCT , CM000677.1:g.28356873_28356881delinsGCTCAGGCT GRCh37
NC_000015.8:g.26030468_26030476delinsGCTCAGGCT NCBI36
NG_016355.1:g.215415_215423delinsAGCCTGAGC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261609.13:c.*28_*36delinsAGCCTGAGC MANE Select ENSP00000261609.8:n.*28_*36delinsAGCCTGAGC
ENST00000650509.1:c.6012_6020delinsAGCCTGAGC ENSP00000496936.1:n.6012_6020delinsAGCCTGAGC
ENST00000261609.11:c.*28_*36delinsAGCCTGAGC ENSP00000261609.7:n.*28_*36delinsAGCCTGAGC
ENST00000566635.5:n.1658_1666delinsAGCCTGAGC
NM_004667.5:c.*28_*36delinsAGCCTGAGC NP_004658.3:n.*28_*36delinsAGCCTGAGC
XM_005268276.3:c.*28_*36delinsAGCCTGAGC XP_005268333.1:n.*28_*36delinsAGCCTGAGC
XM_005268277.3:c.*28_*36delinsAGCCTGAGC XP_005268334.1:n.*28_*36delinsAGCCTGAGC
XM_006720726.2:c.*28_*36delinsAGCCTGAGC XP_006720789.1:n.*28_*36delinsAGCCTGAGC
XM_006720727.2:c.*28_*36delinsAGCCTGAGC XP_006720790.1:n.*28_*36delinsAGCCTGAGC
XM_011522131.1:c.*28_*36delinsAGCCTGAGC XP_011520433.1:n.*28_*36delinsAGCCTGAGC
XM_011522132.1:c.*28_*36delinsAGCCTGAGC XP_011520434.1:n.*28_*36delinsAGCCTGAGC
XM_011522133.1:c.*28_*36delinsAGCCTGAGC XP_011520435.1:n.*28_*36delinsAGCCTGAGC
XM_011522134.1:c.*28_*36delinsAGCCTGAGC XP_011520436.1:n.*28_*36delinsAGCCTGAGC
XM_005268276.5:c.*28_*36delinsAGCCTGAGC XP_005268333.1:n.*28_*36delinsAGCCTGAGC
XM_006720726.3:c.*28_*36delinsAGCCTGAGC XP_006720789.1:n.*28_*36delinsAGCCTGAGC
XM_006720727.3:c.*28_*36delinsAGCCTGAGC XP_006720790.1:n.*28_*36delinsAGCCTGAGC
XM_017022695.1:c.*28_*36delinsAGCCTGAGC XP_016878184.1:n.*28_*36delinsAGCCTGAGC
XM_017022696.1:c.*28_*36delinsAGCCTGAGC XP_016878185.1:n.*28_*36delinsAGCCTGAGC
XM_017022697.1:c.*28_*36delinsAGCCTGAGC XP_016878186.1:n.*28_*36delinsAGCCTGAGC
XM_017022698.1:c.*28_*36delinsAGCCTGAGC XP_016878187.1:n.*28_*36delinsAGCCTGAGC
NM_004667.6:c.*28_*36delinsAGCCTGAGC MANE Select NP_004658.3:n.*28_*36delinsAGCCTGAGC