Canonical Allele Identifier: CA2556794181

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28243768_28243769insAA , CM000677.2:g.28243768_28243769insAA	GRCh38
NC_000015.9:g.28488914_28488915insAA , CM000677.1:g.28488914_28488915insAA	GRCh37
NC_000015.8:g.26162509_26162510insAA	NCBI36
NG_016355.1:g.83381_83382insTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.3577+2112_3577+2113insTT MANE Select	ENSP00000261609.8:n.3577+2112_3577+2113insTT
ENST00000261609.11:c.3577+2112_3577+2113insTT	ENSP00000261609.7:n.3577+2112_3577+2113insTT
NM_004667.5:c.3577+2112_3577+2113insTT	NP_004658.3:n.3577+2112_3577+2113insTT
XM_005268276.3:c.3463+2112_3463+2113insTT	XP_005268333.1:n.3463+2112_3463+2113insTT
XM_005268277.3:c.3463+2112_3463+2113insTT	XP_005268334.1:n.3463+2112_3463+2113insTT
XM_006720726.2:c.3577+2112_3577+2113insTT	XP_006720789.1:n.3577+2112_3577+2113insTT
XM_006720727.2:c.3319+2112_3319+2113insTT	XP_006720790.1:n.3319+2112_3319+2113insTT
XM_011522131.1:c.3094+2112_3094+2113insTT	XP_011520433.1:n.3094+2112_3094+2113insTT
XM_011522132.1:c.1093+2112_1093+2113insTT	XP_011520434.1:n.1093+2112_1093+2113insTT
XM_011522133.1:c.323-4997_323-4996insTT	XP_011520435.1:n.323-4997_323-4996insTT
XM_011522135.1:c.3577+2112_3577+2113insTT	XP_011520437.1:n.3577+2112_3577+2113insTT
XM_011522136.1:c.3577+2112_3577+2113insTT	XP_011520438.1:n.3577+2112_3577+2113insTT
XM_011522137.1:c.3577+2112_3577+2113insTT	XP_011520439.1:n.3577+2112_3577+2113insTT
XR_931930.1:n.3706+2112_3706+2113insTT
XR_931931.1:n.3706+2112_3706+2113insTT
XM_005268276.5:c.3463+2112_3463+2113insTT	XP_005268333.1:n.3463+2112_3463+2113insTT
XM_006720726.3:c.3577+2112_3577+2113insTT	XP_006720789.1:n.3577+2112_3577+2113insTT
XM_006720727.3:c.3319+2112_3319+2113insTT	XP_006720790.1:n.3319+2112_3319+2113insTT
XM_017022695.1:c.3463+2112_3463+2113insTT	XP_016878184.1:n.3463+2112_3463+2113insTT
XM_017022696.1:c.3463+2112_3463+2113insTT	XP_016878185.1:n.3463+2112_3463+2113insTT
XR_001751410.1:n.3707+2112_3707+2113insTT
XR_931930.2:n.3707+2112_3707+2113insTT
NM_004667.6:c.3577+2112_3577+2113insTT MANE Select	NP_004658.3:n.3577+2112_3577+2113insTT