Canonical Allele Identifier: CA2166479867
Gene: HERC2 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28141504G= , CM000677.2:g.28141504G= GRCh38
NC_000015.9:g.28386650G= , CM000677.1:g.28386650G= GRCh37
NC_000015.8:g.26060245G= NCBI36
NG_016355.1:g.185646C=

Transcript Alleles

HGVS Amino-acid change
ENST00000261609.13:c.11943C= MANE Select ENSP00000261609.8:p.Ala3981=
ENST00000650509.1:c.3654C= ENSP00000496936.1:p.Ala1218=
ENST00000261609.11:c.11943C= ENSP00000261609.7:p.Ala3981=
NM_004667.5:c.11943C= NP_004658.3:p.Ala3981=
XM_005268276.3:c.11829C= XP_005268333.1:p.Ala3943=
XM_005268277.3:c.11829C= XP_005268334.1:p.Ala3943=
XM_006720726.2:c.11928C= XP_006720789.1:p.Ala3976=
XM_006720727.2:c.11685C= XP_006720790.1:p.Ala3895=
XM_011522131.1:c.11460C= XP_011520433.1:p.Ala3820=
XM_011522132.1:c.9459C= XP_011520434.1:p.Ala3153=
XM_011522133.1:c.8688C= XP_011520435.1:p.Ala2896=
XM_011522134.1:c.6060C= XP_011520436.1:p.Ala2020=
XM_005268276.5:c.11829C= XP_005268333.1:p.Ala3943=
XM_006720726.3:c.11928C= XP_006720789.1:p.Ala3976=
XM_006720727.3:c.11685C= XP_006720790.1:p.Ala3895=
XM_017022695.1:c.11829C= XP_016878184.1:p.Ala3943=
XM_017022696.1:c.11829C= XP_016878185.1:p.Ala3943=
XM_017022697.1:c.5109C= XP_016878186.1:p.Ala1703=
XM_017022698.1:c.5109C= XP_016878187.1:p.Ala1703=
NM_004667.6:c.11943C= MANE Select NP_004658.3:p.Ala3981=