Canonical Allele Identifier: CA2166480098

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141790A= , CM000677.2:g.28141790A=	GRCh38
NC_000015.9:g.28386936A= , CM000677.1:g.28386936A=	GRCh37
NC_000015.8:g.26060531A=	NCBI36
NG_016355.1:g.185360T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11757T= MANE Select	ENSP00000261609.8:p.His3919=
ENST00000650509.1:c.3468T=	ENSP00000496936.1:p.His1156=
ENST00000261609.11:c.11757T=	ENSP00000261609.7:p.His3919=
ENST00000564519.1:n.272T=
NM_004667.5:c.11757T=	NP_004658.3:p.His3919=
XM_005268276.3:c.11643T=	XP_005268333.1:p.His3881=
XM_005268277.3:c.11643T=	XP_005268334.1:p.His3881=
XM_006720726.2:c.11742T=	XP_006720789.1:p.His3914=
XM_006720727.2:c.11499T=	XP_006720790.1:p.His3833=
XM_011522131.1:c.11274T=	XP_011520433.1:p.His3758=
XM_011522132.1:c.9273T=	XP_011520434.1:p.His3091=
XM_011522133.1:c.8502T=	XP_011520435.1:p.His2834=
XM_011522134.1:c.5874T=	XP_011520436.1:p.His1958=
XM_005268276.5:c.11643T=	XP_005268333.1:p.His3881=
XM_006720726.3:c.11742T=	XP_006720789.1:p.His3914=
XM_006720727.3:c.11499T=	XP_006720790.1:p.His3833=
XM_017022695.1:c.11643T=	XP_016878184.1:p.His3881=
XM_017022696.1:c.11643T=	XP_016878185.1:p.His3881=
XM_017022697.1:c.4923T=	XP_016878186.1:p.His1641=
XM_017022698.1:c.4923T=	XP_016878187.1:p.His1641=
NM_004667.6:c.11757T= MANE Select	NP_004658.3:p.His3919=