Canonical Allele Identifier: CA2166473301
Gene: HERC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28111765A= , CM000677.2:g.28111765A= GRCh38
NC_000015.9:g.28356911A= , CM000677.1:g.28356911A= GRCh37
NC_000015.8:g.26030506A= NCBI36
NG_016355.1:g.215385T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000261609.13:c.14503T= MANE Select ENSP00000261609.8:p.Ter4835=
ENST00000650509.1:c.5982T= ENSP00000496936.1:n.5982T=
ENST00000261609.11:c.14503T= ENSP00000261609.7:p.Ter4835=
ENST00000562136.1:n.629T=
ENST00000566635.5:n.1628T=
NM_004667.5:c.14503T= NP_004658.3:p.Ter4835=
XM_005268276.3:c.14389T= XP_005268333.1:p.Ter4797=
XM_005268277.3:c.14389T= XP_005268334.1:p.Ter4797=
XM_006720726.2:c.14488T= XP_006720789.1:p.Ter4830=
XM_006720727.2:c.14245T= XP_006720790.1:p.Ter4749=
XM_011522131.1:c.14020T= XP_011520433.1:p.Ter4674=
XM_011522132.1:c.12019T= XP_011520434.1:p.Ter4007=
XM_011522133.1:c.11248T= XP_011520435.1:p.Ter3750=
XM_011522134.1:c.8620T= XP_011520436.1:p.Ter2874=
XM_005268276.5:c.14389T= XP_005268333.1:p.Ter4797=
XM_006720726.3:c.14488T= XP_006720789.1:p.Ter4830=
XM_006720727.3:c.14245T= XP_006720790.1:p.Ter4749=
XM_017022695.1:c.14389T= XP_016878184.1:p.Ter4797=
XM_017022696.1:c.14389T= XP_016878185.1:p.Ter4797=
XM_017022697.1:c.7669T= XP_016878186.1:p.Ter2557=
XM_017022698.1:c.7669T= XP_016878187.1:p.Ter2557=
NM_004667.6:c.14503T= MANE Select NP_004658.3:p.Ter4835=