Canonical Allele Identifier: CA2166480097

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141787C= , CM000677.2:g.28141787C=	GRCh38
NC_000015.9:g.28386933C= , CM000677.1:g.28386933C=	GRCh37
NC_000015.8:g.26060528C=	NCBI36
NG_016355.1:g.185363G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11760G= MANE Select	ENSP00000261609.8:p.Glu3920=
ENST00000650509.1:c.3471G=	ENSP00000496936.1:p.Glu1157=
ENST00000261609.11:c.11760G=	ENSP00000261609.7:p.Glu3920=
ENST00000564519.1:n.275G=
NM_004667.5:c.11760G=	NP_004658.3:p.Glu3920=
XM_005268276.3:c.11646G=	XP_005268333.1:p.Glu3882=
XM_005268277.3:c.11646G=	XP_005268334.1:p.Glu3882=
XM_006720726.2:c.11745G=	XP_006720789.1:p.Glu3915=
XM_006720727.2:c.11502G=	XP_006720790.1:p.Glu3834=
XM_011522131.1:c.11277G=	XP_011520433.1:p.Glu3759=
XM_011522132.1:c.9276G=	XP_011520434.1:p.Glu3092=
XM_011522133.1:c.8505G=	XP_011520435.1:p.Glu2835=
XM_011522134.1:c.5877G=	XP_011520436.1:p.Glu1959=
XM_005268276.5:c.11646G=	XP_005268333.1:p.Glu3882=
XM_006720726.3:c.11745G=	XP_006720789.1:p.Glu3915=
XM_006720727.3:c.11502G=	XP_006720790.1:p.Glu3834=
XM_017022695.1:c.11646G=	XP_016878184.1:p.Glu3882=
XM_017022696.1:c.11646G=	XP_016878185.1:p.Glu3882=
XM_017022697.1:c.4926G=	XP_016878186.1:p.Glu1642=
XM_017022698.1:c.4926G=	XP_016878187.1:p.Glu1642=
NM_004667.6:c.11760G= MANE Select	NP_004658.3:p.Glu3920=