Canonical Allele Identifier: CA2166527854
Gene: HERC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28182804_28182812delinsACCAACGTG , CM000677.2:g.28182804_28182812delinsACCAACGTG GRCh38
NC_000015.9:g.28427950_28427958delinsACCAACGTG , CM000677.1:g.28427950_28427958delinsACCAACGTG GRCh37
NC_000015.8:g.26101545_26101553delinsACCAACGTG NCBI36
NG_016355.1:g.144338_144346delinsCACGTTGGT

Transcript Alleles

HGVS Amino-acid change
ENST00000261609.13:c.8826-300_8826-292delinsCACGTTGGT MANE Select ENSP00000261609.8:n.8826-300_8826-292deli...
ENST00000650509.1:c.537-300_537-292delinsCACGTTGGT ENSP00000496936.1:n.537-300_537-292delins...
ENST00000261609.11:c.8826-300_8826-292delinsCACGTTGGT ENSP00000261609.7:n.8826-300_8826-292deli...
NM_004667.5:c.8826-300_8826-292delinsCACGTTGGT NP_004658.3:n.8826-300_8826-292delinsCACG...
XM_005268276.3:c.8712-300_8712-292delinsCACGTTGGT XP_005268333.1:n.8712-300_8712-292delinsC...
XM_005268277.3:c.8712-300_8712-292delinsCACGTTGGT XP_005268334.1:n.8712-300_8712-292delinsC...
XM_006720726.2:c.8811-300_8811-292delinsCACGTTGGT XP_006720789.1:n.8811-300_8811-292delinsC...
XM_006720727.2:c.8568-300_8568-292delinsCACGTTGGT XP_006720790.1:n.8568-300_8568-292delinsC...
XM_011522131.1:c.8343-300_8343-292delinsCACGTTGGT XP_011520433.1:n.8343-300_8343-292delinsC...
XM_011522132.1:c.6342-300_6342-292delinsCACGTTGGT XP_011520434.1:n.6342-300_6342-292delinsC...
XM_011522133.1:c.5571-300_5571-292delinsCACGTTGGT XP_011520435.1:n.5571-300_5571-292delinsC...
XM_011522134.1:c.2943-300_2943-292delinsCACGTTGGT XP_011520436.1:n.2943-300_2943-292delinsC...
XR_931930.1:n.8955-300_8955-292delinsCACGTTGGT
XM_005268276.5:c.8712-300_8712-292delinsCACGTTGGT XP_005268333.1:n.8712-300_8712-292delinsC...
XM_006720726.3:c.8811-300_8811-292delinsCACGTTGGT XP_006720789.1:n.8811-300_8811-292delinsC...
XM_006720727.3:c.8568-300_8568-292delinsCACGTTGGT XP_006720790.1:n.8568-300_8568-292delinsC...
XM_017022695.1:c.8712-300_8712-292delinsCACGTTGGT XP_016878184.1:n.8712-300_8712-292delinsC...
XM_017022696.1:c.8712-300_8712-292delinsCACGTTGGT XP_016878185.1:n.8712-300_8712-292delinsC...
XM_017022697.1:c.1992-300_1992-292delinsCACGTTGGT XP_016878186.1:n.1992-300_1992-292delinsC...
XM_017022698.1:c.1992-300_1992-292delinsCACGTTGGT XP_016878187.1:n.1992-300_1992-292delinsC...
XR_931930.2:n.8956-300_8956-292delinsCACGTTGGT
NM_004667.6:c.8826-300_8826-292delinsCACGTTGGT MANE Select NP_004658.3:n.8826-300_8826-292delinsCACG...