Canonical Allele Identifier: CA2166479909

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141551C= , CM000677.2:g.28141551C=	GRCh38
NC_000015.9:g.28386697C= , CM000677.1:g.28386697C=	GRCh37
NC_000015.8:g.26060292C=	NCBI36
NG_016355.1:g.185599G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11896G= MANE Select	ENSP00000261609.8:p.Gly3966=
ENST00000650509.1:c.3607G=	ENSP00000496936.1:p.Gly1203=
ENST00000261609.11:c.11896G=	ENSP00000261609.7:p.Gly3966=
NM_004667.5:c.11896G=	NP_004658.3:p.Gly3966=
XM_005268276.3:c.11782G=	XP_005268333.1:p.Gly3928=
XM_005268277.3:c.11782G=	XP_005268334.1:p.Gly3928=
XM_006720726.2:c.11881G=	XP_006720789.1:p.Gly3961=
XM_006720727.2:c.11638G=	XP_006720790.1:p.Gly3880=
XM_011522131.1:c.11413G=	XP_011520433.1:p.Gly3805=
XM_011522132.1:c.9412G=	XP_011520434.1:p.Gly3138=
XM_011522133.1:c.8641G=	XP_011520435.1:p.Gly2881=
XM_011522134.1:c.6013G=	XP_011520436.1:p.Gly2005=
XM_005268276.5:c.11782G=	XP_005268333.1:p.Gly3928=
XM_006720726.3:c.11881G=	XP_006720789.1:p.Gly3961=
XM_006720727.3:c.11638G=	XP_006720790.1:p.Gly3880=
XM_017022695.1:c.11782G=	XP_016878184.1:p.Gly3928=
XM_017022696.1:c.11782G=	XP_016878185.1:p.Gly3928=
XM_017022697.1:c.5062G=	XP_016878186.1:p.Gly1688=
XM_017022698.1:c.5062G=	XP_016878187.1:p.Gly1688=
NM_004667.6:c.11896G= MANE Select	NP_004658.3:p.Gly3966=