Canonical Allele Identifier: CA2166566474

Gene: HERC2

Linked Data

• dbSNP Id: rs2076116612

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28284924_28284925insT , CM000677.2:g.28284924_28284925insT	GRCh38
NC_000015.9:g.28530070_28530071insT , CM000677.1:g.28530070_28530071insT	GRCh37
NC_000015.8:g.26203665_26203666insT	NCBI36
NG_016355.1:g.42225_42226insA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.323-4638_323-4637insA MANE Select	ENSP00000261609.8:n.323-4638_323-4637insA
ENST00000261609.11:c.323-4638_323-4637insA	ENSP00000261609.7:n.323-4638_323-4637insA
ENST00000564383.1:n.218-4638_218-4637insA
ENST00000564734.5:c.*193-4638_*193-4637insA	ENSP00000456237.1:n.*193-4638_*193-4637insA
NM_004667.5:c.323-4638_323-4637insA	NP_004658.3:n.323-4638_323-4637insA
XM_005268276.3:c.209-4638_209-4637insA	XP_005268333.1:n.209-4638_209-4637insA
XM_005268277.3:c.209-4638_209-4637insA	XP_005268334.1:n.209-4638_209-4637insA
XM_006720726.2:c.323-4638_323-4637insA	XP_006720789.1:n.323-4638_323-4637insA
XM_006720727.2:c.323-4638_323-4637insA	XP_006720790.1:n.323-4638_323-4637insA
XM_011522133.1:c.322+7963_322+7964insA	XP_011520435.1:n.322+7963_322+7964insA
XM_011522135.1:c.323-4638_323-4637insA	XP_011520437.1:n.323-4638_323-4637insA
XM_011522136.1:c.323-4638_323-4637insA	XP_011520438.1:n.323-4638_323-4637insA
XM_011522137.1:c.323-4638_323-4637insA	XP_011520439.1:n.323-4638_323-4637insA
XR_931930.1:n.452-4638_452-4637insA
XR_931931.1:n.452-4638_452-4637insA
XM_005268276.5:c.209-4638_209-4637insA	XP_005268333.1:n.209-4638_209-4637insA
XM_006720726.3:c.323-4638_323-4637insA	XP_006720789.1:n.323-4638_323-4637insA
XM_006720727.3:c.323-4638_323-4637insA	XP_006720790.1:n.323-4638_323-4637insA
XM_017022695.1:c.209-4638_209-4637insA	XP_016878184.1:n.209-4638_209-4637insA
XM_017022696.1:c.209-4638_209-4637insA	XP_016878185.1:n.209-4638_209-4637insA
XR_001751410.1:n.453-4638_453-4637insA
XR_931930.2:n.453-4638_453-4637insA
NM_004667.6:c.323-4638_323-4637insA MANE Select	NP_004658.3:n.323-4638_323-4637insA