Canonical Allele Identifier: CA2166566579

Gene: HERC2

Linked Data

• dbSNP Id: rs2076122828

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28285122_28285123insGTT , CM000677.2:g.28285122_28285123insGTT	GRCh38
NC_000015.9:g.28530268_28530269insGTT , CM000677.1:g.28530268_28530269insGTT	GRCh37
NC_000015.8:g.26203863_26203864insGTT	NCBI36
NG_016355.1:g.42028_42029insACA

Transcript Alleles

HGVS	Amino-acid change
ENST00000261609.13:c.323-4835_323-4834insACA MANE Select	ENSP00000261609.8:n.323-4835_323-4834insA...
ENST00000261609.11:c.323-4835_323-4834insACA	ENSP00000261609.7:n.323-4835_323-4834insA...
ENST00000564383.1:n.218-4835_218-4834insACA
ENST00000564734.5:c.*193-4835_*193-4834insACA	ENSP00000456237.1:n.*193-4835_*193-4834in...
NM_004667.5:c.323-4835_323-4834insACA	NP_004658.3:n.323-4835_323-4834insACA
XM_005268276.3:c.209-4835_209-4834insACA	XP_005268333.1:n.209-4835_209-4834insACA
XM_005268277.3:c.209-4835_209-4834insACA	XP_005268334.1:n.209-4835_209-4834insACA
XM_006720726.2:c.323-4835_323-4834insACA	XP_006720789.1:n.323-4835_323-4834insACA
XM_006720727.2:c.323-4835_323-4834insACA	XP_006720790.1:n.323-4835_323-4834insACA
XM_011522133.1:c.322+7766_322+7767insACA	XP_011520435.1:n.322+7766_322+7767insACA
XM_011522135.1:c.323-4835_323-4834insACA	XP_011520437.1:n.323-4835_323-4834insACA
XM_011522136.1:c.323-4835_323-4834insACA	XP_011520438.1:n.323-4835_323-4834insACA
XM_011522137.1:c.323-4835_323-4834insACA	XP_011520439.1:n.323-4835_323-4834insACA
XR_931930.1:n.452-4835_452-4834insACA
XR_931931.1:n.452-4835_452-4834insACA
XM_005268276.5:c.209-4835_209-4834insACA	XP_005268333.1:n.209-4835_209-4834insACA
XM_006720726.3:c.323-4835_323-4834insACA	XP_006720789.1:n.323-4835_323-4834insACA
XM_006720727.3:c.323-4835_323-4834insACA	XP_006720790.1:n.323-4835_323-4834insACA
XM_017022695.1:c.209-4835_209-4834insACA	XP_016878184.1:n.209-4835_209-4834insACA
XM_017022696.1:c.209-4835_209-4834insACA	XP_016878185.1:n.209-4835_209-4834insACA
XR_001751410.1:n.453-4835_453-4834insACA
XR_931930.2:n.453-4835_453-4834insACA
NM_004667.6:c.323-4835_323-4834insACA MANE Select	NP_004658.3:n.323-4835_323-4834insACA