Canonical Allele Identifier: CA2166482799
Gene: HERC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28120523_28120527delinsTTTAA , CM000677.2:g.28120523_28120527delinsTTTAA GRCh38
NC_000015.9:g.28365669_28365673delinsTTTAA , CM000677.1:g.28365669_28365673delinsTTTAA GRCh37
NC_000015.8:g.26039264_26039268delinsTTTAA NCBI36
NG_016355.1:g.206623_206627delinsTTAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000261609.13:c.13272+819_13272+823delinsTTAAA MANE Select ENSP00000261609.8:n.13272+819_13272+823de...
ENST00000650509.1:c.4751+819_4751+823delinsTTAAA ENSP00000496936.1:n.4751+819_4751+823deli...
ENST00000261609.11:c.13272+819_13272+823delinsTTAAA ENSP00000261609.7:n.13272+819_13272+823de...
NM_004667.5:c.13272+819_13272+823delinsTTAAA NP_004658.3:n.13272+819_13272+823delinsTT...
XM_005268276.3:c.13158+819_13158+823delinsTTAAA XP_005268333.1:n.13158+819_13158+823delin...
XM_005268277.3:c.13158+819_13158+823delinsTTAAA XP_005268334.1:n.13158+819_13158+823delin...
XM_006720726.2:c.13257+819_13257+823delinsTTAAA XP_006720789.1:n.13257+819_13257+823delin...
XM_006720727.2:c.13014+819_13014+823delinsTTAAA XP_006720790.1:n.13014+819_13014+823delin...
XM_011522131.1:c.12789+819_12789+823delinsTTAAA XP_011520433.1:n.12789+819_12789+823delin...
XM_011522132.1:c.10788+819_10788+823delinsTTAAA XP_011520434.1:n.10788+819_10788+823delin...
XM_011522133.1:c.10017+819_10017+823delinsTTAAA XP_011520435.1:n.10017+819_10017+823delin...
XM_011522134.1:c.7389+819_7389+823delinsTTAAA XP_011520436.1:n.7389+819_7389+823delinsT...
XM_005268276.5:c.13158+819_13158+823delinsTTAAA XP_005268333.1:n.13158+819_13158+823delin...
XM_006720726.3:c.13257+819_13257+823delinsTTAAA XP_006720789.1:n.13257+819_13257+823delin...
XM_006720727.3:c.13014+819_13014+823delinsTTAAA XP_006720790.1:n.13014+819_13014+823delin...
XM_017022695.1:c.13158+819_13158+823delinsTTAAA XP_016878184.1:n.13158+819_13158+823delin...
XM_017022696.1:c.13158+819_13158+823delinsTTAAA XP_016878185.1:n.13158+819_13158+823delin...
XM_017022697.1:c.6438+819_6438+823delinsTTAAA XP_016878186.1:n.6438+819_6438+823delinsT...
XM_017022698.1:c.6438+819_6438+823delinsTTAAA XP_016878187.1:n.6438+819_6438+823delinsT...
NM_004667.6:c.13272+819_13272+823delinsTTAAA MANE Select NP_004658.3:n.13272+819_13272+823delinsTT...