Canonical Allele Identifier: CA2166552659

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28268157_28268158delinsAG , CM000677.2:g.28268157_28268158delinsAG	GRCh38
NC_000015.9:g.28513303_28513304delinsAG , CM000677.1:g.28513303_28513304delinsAG	GRCh37
NC_000015.8:g.26186898_26186899delinsAG	NCBI36
NG_016355.1:g.58992_58993delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.1598+307_1598+308delinsCT MANE Select	ENSP00000261609.8:n.1598+307_1598+308delinsCT
ENST00000261609.11:c.1598+307_1598+308delinsCT	ENSP00000261609.7:n.1598+307_1598+308delinsCT
ENST00000564734.5:c.*1468+307_*1468+308delinsCT	ENSP00000456237.1:n.*1468+307_*1468+308delinsCT
NM_004667.5:c.1598+307_1598+308delinsCT	NP_004658.3:n.1598+307_1598+308delinsCT
XM_005268276.3:c.1484+307_1484+308delinsCT	XP_005268333.1:n.1484+307_1484+308delinsCT
XM_005268277.3:c.1484+307_1484+308delinsCT	XP_005268334.1:n.1484+307_1484+308delinsCT
XM_006720726.2:c.1598+307_1598+308delinsCT	XP_006720789.1:n.1598+307_1598+308delinsCT
XM_006720727.2:c.1340+307_1340+308delinsCT	XP_006720790.1:n.1340+307_1340+308delinsCT
XM_011522131.1:c.1115+307_1115+308delinsCT	XP_011520433.1:n.1115+307_1115+308delinsCT
XM_011522132.1:c.107+4057_107+4058delinsCT	XP_011520434.1:n.107+4057_107+4058delinsCT
XM_011522133.1:c.322+24730_322+24731delinsCT	XP_011520435.1:n.322+24730_322+24731delinsCT
XM_011522135.1:c.1598+307_1598+308delinsCT	XP_011520437.1:n.1598+307_1598+308delinsCT
XM_011522136.1:c.1598+307_1598+308delinsCT	XP_011520438.1:n.1598+307_1598+308delinsCT
XM_011522137.1:c.1598+307_1598+308delinsCT	XP_011520439.1:n.1598+307_1598+308delinsCT
XR_931930.1:n.1727+307_1727+308delinsCT
XR_931931.1:n.1727+307_1727+308delinsCT
XM_005268276.5:c.1484+307_1484+308delinsCT	XP_005268333.1:n.1484+307_1484+308delinsCT
XM_006720726.3:c.1598+307_1598+308delinsCT	XP_006720789.1:n.1598+307_1598+308delinsCT
XM_006720727.3:c.1340+307_1340+308delinsCT	XP_006720790.1:n.1340+307_1340+308delinsCT
XM_017022695.1:c.1484+307_1484+308delinsCT	XP_016878184.1:n.1484+307_1484+308delinsCT
XM_017022696.1:c.1484+307_1484+308delinsCT	XP_016878185.1:n.1484+307_1484+308delinsCT
XR_001751410.1:n.1728+307_1728+308delinsCT
XR_931930.2:n.1728+307_1728+308delinsCT
NM_004667.6:c.1598+307_1598+308delinsCT MANE Select	NP_004658.3:n.1598+307_1598+308delinsCT