Canonical Allele Identifier: CA2166479831

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141456G= , CM000677.2:g.28141456G=	GRCh38
NC_000015.9:g.28386602G= , CM000677.1:g.28386602G=	GRCh37
NC_000015.8:g.26060197G=	NCBI36
NG_016355.1:g.185694C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11991C= MANE Select	ENSP00000261609.8:p.Leu3997=
ENST00000650509.1:c.3702C=	ENSP00000496936.1:p.Leu1234=
ENST00000261609.11:c.11991C=	ENSP00000261609.7:p.Leu3997=
NM_004667.5:c.11991C=	NP_004658.3:p.Leu3997=
XM_005268276.3:c.11877C=	XP_005268333.1:p.Leu3959=
XM_005268277.3:c.11877C=	XP_005268334.1:p.Leu3959=
XM_006720726.2:c.11976C=	XP_006720789.1:p.Leu3992=
XM_006720727.2:c.11733C=	XP_006720790.1:p.Leu3911=
XM_011522131.1:c.11508C=	XP_011520433.1:p.Leu3836=
XM_011522132.1:c.9507C=	XP_011520434.1:p.Leu3169=
XM_011522133.1:c.8736C=	XP_011520435.1:p.Leu2912=
XM_011522134.1:c.6108C=	XP_011520436.1:p.Leu2036=
XM_005268276.5:c.11877C=	XP_005268333.1:p.Leu3959=
XM_006720726.3:c.11976C=	XP_006720789.1:p.Leu3992=
XM_006720727.3:c.11733C=	XP_006720790.1:p.Leu3911=
XM_017022695.1:c.11877C=	XP_016878184.1:p.Leu3959=
XM_017022696.1:c.11877C=	XP_016878185.1:p.Leu3959=
XM_017022697.1:c.5157C=	XP_016878186.1:p.Leu1719=
XM_017022698.1:c.5157C=	XP_016878187.1:p.Leu1719=
NM_004667.6:c.11991C= MANE Select	NP_004658.3:p.Leu3997=