Canonical Allele Identifier: CA2166479859

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141496G= , CM000677.2:g.28141496G=	GRCh38
NC_000015.9:g.28386642G= , CM000677.1:g.28386642G=	GRCh37
NC_000015.8:g.26060237G=	NCBI36
NG_016355.1:g.185654C=

Transcript Alleles

HGVS	Amino-acid change
ENST00000261609.13:c.11951C= MANE Select	ENSP00000261609.8:p.Thr3984=
ENST00000650509.1:c.3662C=	ENSP00000496936.1:p.Thr1221=
ENST00000261609.11:c.11951C=	ENSP00000261609.7:p.Thr3984=
NM_004667.5:c.11951C=	NP_004658.3:p.Thr3984=
XM_005268276.3:c.11837C=	XP_005268333.1:p.Thr3946=
XM_005268277.3:c.11837C=	XP_005268334.1:p.Thr3946=
XM_006720726.2:c.11936C=	XP_006720789.1:p.Thr3979=
XM_006720727.2:c.11693C=	XP_006720790.1:p.Thr3898=
XM_011522131.1:c.11468C=	XP_011520433.1:p.Thr3823=
XM_011522132.1:c.9467C=	XP_011520434.1:p.Thr3156=
XM_011522133.1:c.8696C=	XP_011520435.1:p.Thr2899=
XM_011522134.1:c.6068C=	XP_011520436.1:p.Thr2023=
XM_005268276.5:c.11837C=	XP_005268333.1:p.Thr3946=
XM_006720726.3:c.11936C=	XP_006720789.1:p.Thr3979=
XM_006720727.3:c.11693C=	XP_006720790.1:p.Thr3898=
XM_017022695.1:c.11837C=	XP_016878184.1:p.Thr3946=
XM_017022696.1:c.11837C=	XP_016878185.1:p.Thr3946=
XM_017022697.1:c.5117C=	XP_016878186.1:p.Thr1706=
XM_017022698.1:c.5117C=	XP_016878187.1:p.Thr1706=
NM_004667.6:c.11951C= MANE Select	NP_004658.3:p.Thr3984=