Canonical Allele Identifier: CA2730503992

Gene: HERC2

Linked Data

• dbSNP Id: rs2141082518

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28284949_28284950insAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000677.2:g.28284949_28284950insAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	GRCh38
NC_000015.9:g.28530095_28530096insAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAA , CM000677.1:g.28530095_28530096insAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	GRCh37
NC_000015.8:g.26203690_26203691insAAAAAAACAAAAAAAAAAAAAAAAAAAAAAAAAAAAA	NCBI36
NG_016355.1:g.42229_42230insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	ENSP00000261609.8:n.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTT...
ENST00000261609.11:c.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000261609.7:n.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTT...
ENST00000564383.1:n.218-4634_218-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
ENST00000564734.5:c.*193-4634_*193-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	ENSP00000456237.1:n.*193-4634_*193-4633insGTTTTTTTTTTTTTTTTTT...
NM_004667.5:c.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	NP_004658.3:n.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTT...
XM_005268276.3:c.209-4634_209-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_005268333.1:n.209-4634_209-4633insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_005268277.3:c.209-4634_209-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_005268334.1:n.209-4634_209-4633insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_006720726.2:c.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_006720789.1:n.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_006720727.2:c.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_006720790.1:n.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_011522133.1:c.322+7967_322+7968insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_011520435.1:n.322+7967_322+7968insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_011522135.1:c.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_011520437.1:n.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_011522136.1:c.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_011520438.1:n.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_011522137.1:c.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_011520439.1:n.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTTTTT...
XR_931930.1:n.452-4634_452-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XR_931931.1:n.452-4634_452-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XM_005268276.5:c.209-4634_209-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_005268333.1:n.209-4634_209-4633insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_006720726.3:c.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_006720789.1:n.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_006720727.3:c.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_006720790.1:n.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_017022695.1:c.209-4634_209-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_016878184.1:n.209-4634_209-4633insGTTTTTTTTTTTTTTTTTTTTTTT...
XM_017022696.1:c.209-4634_209-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT	XP_016878185.1:n.209-4634_209-4633insGTTTTTTTTTTTTTTTTTTTTTTT...
XR_001751410.1:n.453-4634_453-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
XR_931930.2:n.453-4634_453-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT
NM_004667.6:c.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTTT MANE Select	NP_004658.3:n.323-4634_323-4633insGTTTTTTTTTTTTTTTTTTTTTTTTTT...