Canonical Allele Identifier: CA2166482708
Gene: HERC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28120325_28120327delinsGTA , CM000677.2:g.28120325_28120327delinsGTA GRCh38
NC_000015.9:g.28365471_28365473delinsGTA , CM000677.1:g.28365471_28365473delinsGTA GRCh37
NC_000015.8:g.26039066_26039068delinsGTA NCBI36
NG_016355.1:g.206823_206825delinsTAC

Transcript Alleles

HGVS Amino-acid Change
ENST00000261609.13:c.13272+1019_13272+1021delinsTAC MANE Select ENSP00000261609.8:n.13272+1019_13272+1021delinsTAC
ENST00000650509.1:c.4751+1019_4751+1021delinsTAC ENSP00000496936.1:n.4751+1019_4751+1021delinsTAC
ENST00000261609.11:c.13272+1019_13272+1021delinsTAC ENSP00000261609.7:n.13272+1019_13272+1021delinsTAC
NM_004667.5:c.13272+1019_13272+1021delinsTAC NP_004658.3:n.13272+1019_13272+1021delinsTAC
XM_005268276.3:c.13158+1019_13158+1021delinsTAC XP_005268333.1:n.13158+1019_13158+1021delinsTAC
XM_005268277.3:c.13158+1019_13158+1021delinsTAC XP_005268334.1:n.13158+1019_13158+1021delinsTAC
XM_006720726.2:c.13257+1019_13257+1021delinsTAC XP_006720789.1:n.13257+1019_13257+1021delinsTAC
XM_006720727.2:c.13014+1019_13014+1021delinsTAC XP_006720790.1:n.13014+1019_13014+1021delinsTAC
XM_011522131.1:c.12789+1019_12789+1021delinsTAC XP_011520433.1:n.12789+1019_12789+1021delinsTAC
XM_011522132.1:c.10788+1019_10788+1021delinsTAC XP_011520434.1:n.10788+1019_10788+1021delinsTAC
XM_011522133.1:c.10017+1019_10017+1021delinsTAC XP_011520435.1:n.10017+1019_10017+1021delinsTAC
XM_011522134.1:c.7389+1019_7389+1021delinsTAC XP_011520436.1:n.7389+1019_7389+1021delinsTAC
XM_005268276.5:c.13158+1019_13158+1021delinsTAC XP_005268333.1:n.13158+1019_13158+1021delinsTAC
XM_006720726.3:c.13257+1019_13257+1021delinsTAC XP_006720789.1:n.13257+1019_13257+1021delinsTAC
XM_006720727.3:c.13014+1019_13014+1021delinsTAC XP_006720790.1:n.13014+1019_13014+1021delinsTAC
XM_017022695.1:c.13158+1019_13158+1021delinsTAC XP_016878184.1:n.13158+1019_13158+1021delinsTAC
XM_017022696.1:c.13158+1019_13158+1021delinsTAC XP_016878185.1:n.13158+1019_13158+1021delinsTAC
XM_017022697.1:c.6438+1019_6438+1021delinsTAC XP_016878186.1:n.6438+1019_6438+1021delinsTAC
XM_017022698.1:c.6438+1019_6438+1021delinsTAC XP_016878187.1:n.6438+1019_6438+1021delinsTAC
NM_004667.6:c.13272+1019_13272+1021delinsTAC MANE Select NP_004658.3:n.13272+1019_13272+1021delinsTAC