Canonical Allele Identifier: CA2166479890

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141533T= , CM000677.2:g.28141533T=	GRCh38
NC_000015.9:g.28386679T= , CM000677.1:g.28386679T=	GRCh37
NC_000015.8:g.26060274T=	NCBI36
NG_016355.1:g.185617A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11914A= MANE Select	ENSP00000261609.8:p.Lys3972=
ENST00000650509.1:c.3625A=	ENSP00000496936.1:p.Lys1209=
ENST00000261609.11:c.11914A=	ENSP00000261609.7:p.Lys3972=
NM_004667.5:c.11914A=	NP_004658.3:p.Lys3972=
XM_005268276.3:c.11800A=	XP_005268333.1:p.Lys3934=
XM_005268277.3:c.11800A=	XP_005268334.1:p.Lys3934=
XM_006720726.2:c.11899A=	XP_006720789.1:p.Lys3967=
XM_006720727.2:c.11656A=	XP_006720790.1:p.Lys3886=
XM_011522131.1:c.11431A=	XP_011520433.1:p.Lys3811=
XM_011522132.1:c.9430A=	XP_011520434.1:p.Lys3144=
XM_011522133.1:c.8659A=	XP_011520435.1:p.Lys2887=
XM_011522134.1:c.6031A=	XP_011520436.1:p.Lys2011=
XM_005268276.5:c.11800A=	XP_005268333.1:p.Lys3934=
XM_006720726.3:c.11899A=	XP_006720789.1:p.Lys3967=
XM_006720727.3:c.11656A=	XP_006720790.1:p.Lys3886=
XM_017022695.1:c.11800A=	XP_016878184.1:p.Lys3934=
XM_017022696.1:c.11800A=	XP_016878185.1:p.Lys3934=
XM_017022697.1:c.5080A=	XP_016878186.1:p.Lys1694=
XM_017022698.1:c.5080A=	XP_016878187.1:p.Lys1694=
NM_004667.6:c.11914A= MANE Select	NP_004658.3:p.Lys3972=