Canonical Allele Identifier: CA2803514279

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28284918_28284919insC , CM000677.2:g.28284918_28284919insC	GRCh38
NC_000015.9:g.28530064_28530065insC , CM000677.1:g.28530064_28530065insC	GRCh37
NC_000015.8:g.26203659_26203660insC	NCBI36
NG_016355.1:g.42231_42232insG

Transcript Alleles

HGVS	Amino-acid change
ENST00000261609.13:c.323-4632_323-4631insG MANE Select	ENSP00000261609.8:n.323-4632_323-4631insG
ENST00000261609.11:c.323-4632_323-4631insG	ENSP00000261609.7:n.323-4632_323-4631insG
ENST00000564383.1:n.218-4632_218-4631insG
ENST00000564734.5:c.*193-4632_*193-4631insG	ENSP00000456237.1:n.*193-4632_*193-4631insG
NM_004667.5:c.323-4632_323-4631insG	NP_004658.3:n.323-4632_323-4631insG
XM_005268276.3:c.209-4632_209-4631insG	XP_005268333.1:n.209-4632_209-4631insG
XM_005268277.3:c.209-4632_209-4631insG	XP_005268334.1:n.209-4632_209-4631insG
XM_006720726.2:c.323-4632_323-4631insG	XP_006720789.1:n.323-4632_323-4631insG
XM_006720727.2:c.323-4632_323-4631insG	XP_006720790.1:n.323-4632_323-4631insG
XM_011522133.1:c.322+7969_322+7970insG	XP_011520435.1:n.322+7969_322+7970insG
XM_011522135.1:c.323-4632_323-4631insG	XP_011520437.1:n.323-4632_323-4631insG
XM_011522136.1:c.323-4632_323-4631insG	XP_011520438.1:n.323-4632_323-4631insG
XM_011522137.1:c.323-4632_323-4631insG	XP_011520439.1:n.323-4632_323-4631insG
XR_931930.1:n.452-4632_452-4631insG
XR_931931.1:n.452-4632_452-4631insG
XM_005268276.5:c.209-4632_209-4631insG	XP_005268333.1:n.209-4632_209-4631insG
XM_006720726.3:c.323-4632_323-4631insG	XP_006720789.1:n.323-4632_323-4631insG
XM_006720727.3:c.323-4632_323-4631insG	XP_006720790.1:n.323-4632_323-4631insG
XM_017022695.1:c.209-4632_209-4631insG	XP_016878184.1:n.209-4632_209-4631insG
XM_017022696.1:c.209-4632_209-4631insG	XP_016878185.1:n.209-4632_209-4631insG
XR_001751410.1:n.453-4632_453-4631insG
XR_931930.2:n.453-4632_453-4631insG
NM_004667.6:c.323-4632_323-4631insG MANE Select	NP_004658.3:n.323-4632_323-4631insG