Canonical Allele Identifier: CA2166479932

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141581C= , CM000677.2:g.28141581C=	GRCh38
NC_000015.9:g.28386727C= , CM000677.1:g.28386727C=	GRCh37
NC_000015.8:g.26060322C=	NCBI36
NG_016355.1:g.185569G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11866G= MANE Select	ENSP00000261609.8:p.Gly3956=
ENST00000650509.1:c.3577G=	ENSP00000496936.1:p.Gly1193=
ENST00000261609.11:c.11866G=	ENSP00000261609.7:p.Gly3956=
NM_004667.5:c.11866G=	NP_004658.3:p.Gly3956=
XM_005268276.3:c.11752G=	XP_005268333.1:p.Gly3918=
XM_005268277.3:c.11752G=	XP_005268334.1:p.Gly3918=
XM_006720726.2:c.11851G=	XP_006720789.1:p.Gly3951=
XM_006720727.2:c.11608G=	XP_006720790.1:p.Gly3870=
XM_011522131.1:c.11383G=	XP_011520433.1:p.Gly3795=
XM_011522132.1:c.9382G=	XP_011520434.1:p.Gly3128=
XM_011522133.1:c.8611G=	XP_011520435.1:p.Gly2871=
XM_011522134.1:c.5983G=	XP_011520436.1:p.Gly1995=
XM_005268276.5:c.11752G=	XP_005268333.1:p.Gly3918=
XM_006720726.3:c.11851G=	XP_006720789.1:p.Gly3951=
XM_006720727.3:c.11608G=	XP_006720790.1:p.Gly3870=
XM_017022695.1:c.11752G=	XP_016878184.1:p.Gly3918=
XM_017022696.1:c.11752G=	XP_016878185.1:p.Gly3918=
XM_017022697.1:c.5032G=	XP_016878186.1:p.Gly1678=
XM_017022698.1:c.5032G=	XP_016878187.1:p.Gly1678=
NM_004667.6:c.11866G= MANE Select	NP_004658.3:p.Gly3956=