Canonical Allele Identifier: CA2166480107

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141810C= , CM000677.2:g.28141810C=	GRCh38
NC_000015.9:g.28386956C= , CM000677.1:g.28386956C=	GRCh37
NC_000015.8:g.26060551C=	NCBI36
NG_016355.1:g.185340G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11737G= MANE Select	ENSP00000261609.8:p.Glu3913=
ENST00000650509.1:c.3448G=	ENSP00000496936.1:p.Glu1150=
ENST00000261609.11:c.11737G=	ENSP00000261609.7:p.Glu3913=
ENST00000564519.1:n.252G=
NM_004667.5:c.11737G=	NP_004658.3:p.Glu3913=
XM_005268276.3:c.11623G=	XP_005268333.1:p.Glu3875=
XM_005268277.3:c.11623G=	XP_005268334.1:p.Glu3875=
XM_006720726.2:c.11722G=	XP_006720789.1:p.Glu3908=
XM_006720727.2:c.11479G=	XP_006720790.1:p.Glu3827=
XM_011522131.1:c.11254G=	XP_011520433.1:p.Glu3752=
XM_011522132.1:c.9253G=	XP_011520434.1:p.Glu3085=
XM_011522133.1:c.8482G=	XP_011520435.1:p.Glu2828=
XM_011522134.1:c.5854G=	XP_011520436.1:p.Glu1952=
XM_005268276.5:c.11623G=	XP_005268333.1:p.Glu3875=
XM_006720726.3:c.11722G=	XP_006720789.1:p.Glu3908=
XM_006720727.3:c.11479G=	XP_006720790.1:p.Glu3827=
XM_017022695.1:c.11623G=	XP_016878184.1:p.Glu3875=
XM_017022696.1:c.11623G=	XP_016878185.1:p.Glu3875=
XM_017022697.1:c.4903G=	XP_016878186.1:p.Glu1635=
XM_017022698.1:c.4903G=	XP_016878187.1:p.Glu1635=
NM_004667.6:c.11737G= MANE Select	NP_004658.3:p.Glu3913=