Canonical Allele Identifier: CA2166479928

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141573T= , CM000677.2:g.28141573T=	GRCh38
NC_000015.9:g.28386719T= , CM000677.1:g.28386719T=	GRCh37
NC_000015.8:g.26060314T=	NCBI36
NG_016355.1:g.185577A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11874A= MANE Select	ENSP00000261609.8:p.Gly3958=
ENST00000650509.1:c.3585A=	ENSP00000496936.1:p.Gly1195=
ENST00000261609.11:c.11874A=	ENSP00000261609.7:p.Gly3958=
NM_004667.5:c.11874A=	NP_004658.3:p.Gly3958=
XM_005268276.3:c.11760A=	XP_005268333.1:p.Gly3920=
XM_005268277.3:c.11760A=	XP_005268334.1:p.Gly3920=
XM_006720726.2:c.11859A=	XP_006720789.1:p.Gly3953=
XM_006720727.2:c.11616A=	XP_006720790.1:p.Gly3872=
XM_011522131.1:c.11391A=	XP_011520433.1:p.Gly3797=
XM_011522132.1:c.9390A=	XP_011520434.1:p.Gly3130=
XM_011522133.1:c.8619A=	XP_011520435.1:p.Gly2873=
XM_011522134.1:c.5991A=	XP_011520436.1:p.Gly1997=
XM_005268276.5:c.11760A=	XP_005268333.1:p.Gly3920=
XM_006720726.3:c.11859A=	XP_006720789.1:p.Gly3953=
XM_006720727.3:c.11616A=	XP_006720790.1:p.Gly3872=
XM_017022695.1:c.11760A=	XP_016878184.1:p.Gly3920=
XM_017022696.1:c.11760A=	XP_016878185.1:p.Gly3920=
XM_017022697.1:c.5040A=	XP_016878186.1:p.Gly1680=
XM_017022698.1:c.5040A=	XP_016878187.1:p.Gly1680=
NM_004667.6:c.11874A= MANE Select	NP_004658.3:p.Gly3958=