Canonical Allele Identifier: CA2166480102

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141796A= , CM000677.2:g.28141796A=	GRCh38
NC_000015.9:g.28386942A= , CM000677.1:g.28386942A=	GRCh37
NC_000015.8:g.26060537A=	NCBI36
NG_016355.1:g.185354T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11751T= MANE Select	ENSP00000261609.8:p.Val3917=
ENST00000650509.1:c.3462T=	ENSP00000496936.1:p.Val1154=
ENST00000261609.11:c.11751T=	ENSP00000261609.7:p.Val3917=
ENST00000564519.1:n.266T=
NM_004667.5:c.11751T=	NP_004658.3:p.Val3917=
XM_005268276.3:c.11637T=	XP_005268333.1:p.Val3879=
XM_005268277.3:c.11637T=	XP_005268334.1:p.Val3879=
XM_006720726.2:c.11736T=	XP_006720789.1:p.Val3912=
XM_006720727.2:c.11493T=	XP_006720790.1:p.Val3831=
XM_011522131.1:c.11268T=	XP_011520433.1:p.Val3756=
XM_011522132.1:c.9267T=	XP_011520434.1:p.Val3089=
XM_011522133.1:c.8496T=	XP_011520435.1:p.Val2832=
XM_011522134.1:c.5868T=	XP_011520436.1:p.Val1956=
XM_005268276.5:c.11637T=	XP_005268333.1:p.Val3879=
XM_006720726.3:c.11736T=	XP_006720789.1:p.Val3912=
XM_006720727.3:c.11493T=	XP_006720790.1:p.Val3831=
XM_017022695.1:c.11637T=	XP_016878184.1:p.Val3879=
XM_017022696.1:c.11637T=	XP_016878185.1:p.Val3879=
XM_017022697.1:c.4917T=	XP_016878186.1:p.Val1639=
XM_017022698.1:c.4917T=	XP_016878187.1:p.Val1639=
NM_004667.6:c.11751T= MANE Select	NP_004658.3:p.Val3917=