Canonical Allele Identifier: CA2166479925

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141564G= , CM000677.2:g.28141564G=	GRCh38
NC_000015.9:g.28386710G= , CM000677.1:g.28386710G=	GRCh37
NC_000015.8:g.26060305G=	NCBI36
NG_016355.1:g.185586C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11883C= MANE Select	ENSP00000261609.8:p.His3961=
ENST00000650509.1:c.3594C=	ENSP00000496936.1:p.His1198=
ENST00000261609.11:c.11883C=	ENSP00000261609.7:p.His3961=
NM_004667.5:c.11883C=	NP_004658.3:p.His3961=
XM_005268276.3:c.11769C=	XP_005268333.1:p.His3923=
XM_005268277.3:c.11769C=	XP_005268334.1:p.His3923=
XM_006720726.2:c.11868C=	XP_006720789.1:p.His3956=
XM_006720727.2:c.11625C=	XP_006720790.1:p.His3875=
XM_011522131.1:c.11400C=	XP_011520433.1:p.His3800=
XM_011522132.1:c.9399C=	XP_011520434.1:p.His3133=
XM_011522133.1:c.8628C=	XP_011520435.1:p.His2876=
XM_011522134.1:c.6000C=	XP_011520436.1:p.His2000=
XM_005268276.5:c.11769C=	XP_005268333.1:p.His3923=
XM_006720726.3:c.11868C=	XP_006720789.1:p.His3956=
XM_006720727.3:c.11625C=	XP_006720790.1:p.His3875=
XM_017022695.1:c.11769C=	XP_016878184.1:p.His3923=
XM_017022696.1:c.11769C=	XP_016878185.1:p.His3923=
XM_017022697.1:c.5049C=	XP_016878186.1:p.His1683=
XM_017022698.1:c.5049C=	XP_016878187.1:p.His1683=
NM_004667.6:c.11883C= MANE Select	NP_004658.3:p.His3961=