Canonical Allele Identifier: CA2166479820
Gene: HERC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28141444C= , CM000677.2:g.28141444C= GRCh38
NC_000015.9:g.28386590C= , CM000677.1:g.28386590C= GRCh37
NC_000015.8:g.26060185C= NCBI36
NG_016355.1:g.185706G=

Transcript Alleles

HGVS Amino-acid change
ENST00000261609.13:c.12003G= MANE Select ENSP00000261609.8:p.Thr4001=
ENST00000650509.1:c.3714G= ENSP00000496936.1:p.Thr1238=
ENST00000261609.11:c.12003G= ENSP00000261609.7:p.Thr4001=
NM_004667.5:c.12003G= NP_004658.3:p.Thr4001=
XM_005268276.3:c.11889G= XP_005268333.1:p.Thr3963=
XM_005268277.3:c.11889G= XP_005268334.1:p.Thr3963=
XM_006720726.2:c.11988G= XP_006720789.1:p.Thr3996=
XM_006720727.2:c.11745G= XP_006720790.1:p.Thr3915=
XM_011522131.1:c.11520G= XP_011520433.1:p.Thr3840=
XM_011522132.1:c.9519G= XP_011520434.1:p.Thr3173=
XM_011522133.1:c.8748G= XP_011520435.1:p.Thr2916=
XM_011522134.1:c.6120G= XP_011520436.1:p.Thr2040=
XM_005268276.5:c.11889G= XP_005268333.1:p.Thr3963=
XM_006720726.3:c.11988G= XP_006720789.1:p.Thr3996=
XM_006720727.3:c.11745G= XP_006720790.1:p.Thr3915=
XM_017022695.1:c.11889G= XP_016878184.1:p.Thr3963=
XM_017022696.1:c.11889G= XP_016878185.1:p.Thr3963=
XM_017022697.1:c.5169G= XP_016878186.1:p.Thr1723=
XM_017022698.1:c.5169G= XP_016878187.1:p.Thr1723=
NM_004667.6:c.12003G= MANE Select NP_004658.3:p.Thr4001=