Canonical Allele Identifier: CA968024289

Gene: HERC2

Linked Data

• gnomAD v3: 15-28182840-T-TGCTACAAATGGCACTGAATGATTCCCACCCATGAATCATTCCAAGCCAA
• gnomAD v4: 15-28182840-T-TGCTACAAATGGCACTGAATGATTCCCACCCATGAATCATTCCAAGCCAA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28182841_28182842insCTACAAATGGCACTGAATGATTCCCACCCATGAATCATTCCAAGCCAAG , CM000677.2:g.28182841_28182842insCTACAAATGGCACTGAATGATTCCCACCCATGAATCATTCCAAGCCAAG	GRCh38
NC_000015.9:g.28427987_28427988insCTACAAATGGCACTGAATGATTCCCACCCATGAATCATTCCAAGCCAAG , CM000677.1:g.28427987_28427988insCTACAAATGGCACTGAATGATTCCCACCCATGAATCATTCCAAGCCAAG	GRCh37
NC_000015.8:g.26101582_26101583insCTACAAATGGCACTGAATGATTCCCACCCATGAATCATTCCAAGCCAAG	NCBI36
NG_016355.1:g.144309_144310insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.8826-329_8826-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC MANE Select	ENSP00000261609.8:n.8826-329_8826-328insTTGGCTTGGAATGATTCATGG...
ENST00000650509.1:c.537-329_537-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC	ENSP00000496936.1:n.537-329_537-328insTTGGCTTGGAATGATTCATGGGT...
ENST00000261609.11:c.8826-329_8826-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC	ENSP00000261609.7:n.8826-329_8826-328insTTGGCTTGGAATGATTCATGG...
NM_004667.5:c.8826-329_8826-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC	NP_004658.3:n.8826-329_8826-328insTTGGCTTGGAATGATTCATGGGTGGGA...
XM_005268276.3:c.8712-329_8712-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC	XP_005268333.1:n.8712-329_8712-328insTTGGCTTGGAATGATTCATGGGTG...
XM_005268277.3:c.8712-329_8712-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC	XP_005268334.1:n.8712-329_8712-328insTTGGCTTGGAATGATTCATGGGTG...
XM_006720726.2:c.8811-329_8811-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC	XP_006720789.1:n.8811-329_8811-328insTTGGCTTGGAATGATTCATGGGTG...
XM_006720727.2:c.8568-329_8568-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC	XP_006720790.1:n.8568-329_8568-328insTTGGCTTGGAATGATTCATGGGTG...
XM_011522131.1:c.8343-329_8343-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC	XP_011520433.1:n.8343-329_8343-328insTTGGCTTGGAATGATTCATGGGTG...
XM_011522132.1:c.6342-329_6342-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC	XP_011520434.1:n.6342-329_6342-328insTTGGCTTGGAATGATTCATGGGTG...
XM_011522133.1:c.5571-329_5571-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC	XP_011520435.1:n.5571-329_5571-328insTTGGCTTGGAATGATTCATGGGTG...
XM_011522134.1:c.2943-329_2943-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC	XP_011520436.1:n.2943-329_2943-328insTTGGCTTGGAATGATTCATGGGTG...
XR_931930.1:n.8955-329_8955-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC
XM_005268276.5:c.8712-329_8712-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC	XP_005268333.1:n.8712-329_8712-328insTTGGCTTGGAATGATTCATGGGTG...
XM_006720726.3:c.8811-329_8811-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC	XP_006720789.1:n.8811-329_8811-328insTTGGCTTGGAATGATTCATGGGTG...
XM_006720727.3:c.8568-329_8568-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC	XP_006720790.1:n.8568-329_8568-328insTTGGCTTGGAATGATTCATGGGTG...
XM_017022695.1:c.8712-329_8712-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC	XP_016878184.1:n.8712-329_8712-328insTTGGCTTGGAATGATTCATGGGTG...
XM_017022696.1:c.8712-329_8712-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC	XP_016878185.1:n.8712-329_8712-328insTTGGCTTGGAATGATTCATGGGTG...
XM_017022697.1:c.1992-329_1992-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC	XP_016878186.1:n.1992-329_1992-328insTTGGCTTGGAATGATTCATGGGTG...
XM_017022698.1:c.1992-329_1992-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC	XP_016878187.1:n.1992-329_1992-328insTTGGCTTGGAATGATTCATGGGTG...
XR_931930.2:n.8956-329_8956-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC
NM_004667.6:c.8826-329_8826-328insTTGGCTTGGAATGATTCATGGGTGGGAATCATTCAGTGCCATTTGTAGC MANE Select	NP_004658.3:n.8826-329_8826-328insTTGGCTTGGAATGATTCATGGGTGGGA...