Canonical Allele Identifier: CA2803510924

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141636_28141637insCCCCCCAAACACACCC , CM000677.2:g.28141636_28141637insCCCCCCAAACACACCC	GRCh38
NC_000015.9:g.28386782_28386783insCCCCCCAAACACACCC , CM000677.1:g.28386782_28386783insCCCCCCAAACACACCC	GRCh37
NC_000015.8:g.26060377_26060378insCCCCCCAAACACACCC	NCBI36
NG_016355.1:g.185513_185514insGGGTGTGTTTGGGGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11817-7_11817-6insGGGTGTGTTTGGGGGG MANE Select	ENSP00000261609.8:n.11817-7_11817-6insGGGTGTGTTTGGGGGG
ENST00000650509.1:c.3528-7_3528-6insGGGTGTGTTTGGGGGG	ENSP00000496936.1:n.3528-7_3528-6insGGGTGTGTTTGGGGGG
ENST00000261609.11:c.11817-7_11817-6insGGGTGTGTTTGGGGGG	ENSP00000261609.7:n.11817-7_11817-6insGGGTGTGTTTGGGGGG
NM_004667.5:c.11817-7_11817-6insGGGTGTGTTTGGGGGG	NP_004658.3:n.11817-7_11817-6insGGGTGTGTTTGGGGGG
XM_005268276.3:c.11703-7_11703-6insGGGTGTGTTTGGGGGG	XP_005268333.1:n.11703-7_11703-6insGGGTGTGTTTGGGGGG
XM_005268277.3:c.11703-7_11703-6insGGGTGTGTTTGGGGGG	XP_005268334.1:n.11703-7_11703-6insGGGTGTGTTTGGGGGG
XM_006720726.2:c.11802-7_11802-6insGGGTGTGTTTGGGGGG	XP_006720789.1:n.11802-7_11802-6insGGGTGTGTTTGGGGGG
XM_006720727.2:c.11559-7_11559-6insGGGTGTGTTTGGGGGG	XP_006720790.1:n.11559-7_11559-6insGGGTGTGTTTGGGGGG
XM_011522131.1:c.11334-7_11334-6insGGGTGTGTTTGGGGGG	XP_011520433.1:n.11334-7_11334-6insGGGTGTGTTTGGGGGG
XM_011522132.1:c.9333-7_9333-6insGGGTGTGTTTGGGGGG	XP_011520434.1:n.9333-7_9333-6insGGGTGTGTTTGGGGGG
XM_011522133.1:c.8562-7_8562-6insGGGTGTGTTTGGGGGG	XP_011520435.1:n.8562-7_8562-6insGGGTGTGTTTGGGGGG
XM_011522134.1:c.5934-7_5934-6insGGGTGTGTTTGGGGGG	XP_011520436.1:n.5934-7_5934-6insGGGTGTGTTTGGGGGG
XM_005268276.5:c.11703-7_11703-6insGGGTGTGTTTGGGGGG	XP_005268333.1:n.11703-7_11703-6insGGGTGTGTTTGGGGGG
XM_006720726.3:c.11802-7_11802-6insGGGTGTGTTTGGGGGG	XP_006720789.1:n.11802-7_11802-6insGGGTGTGTTTGGGGGG
XM_006720727.3:c.11559-7_11559-6insGGGTGTGTTTGGGGGG	XP_006720790.1:n.11559-7_11559-6insGGGTGTGTTTGGGGGG
XM_017022695.1:c.11703-7_11703-6insGGGTGTGTTTGGGGGG	XP_016878184.1:n.11703-7_11703-6insGGGTGTGTTTGGGGGG
XM_017022696.1:c.11703-7_11703-6insGGGTGTGTTTGGGGGG	XP_016878185.1:n.11703-7_11703-6insGGGTGTGTTTGGGGGG
XM_017022697.1:c.4983-7_4983-6insGGGTGTGTTTGGGGGG	XP_016878186.1:n.4983-7_4983-6insGGGTGTGTTTGGGGGG
XM_017022698.1:c.4983-7_4983-6insGGGTGTGTTTGGGGGG	XP_016878187.1:n.4983-7_4983-6insGGGTGTGTTTGGGGGG
NM_004667.6:c.11817-7_11817-6insGGGTGTGTTTGGGGGG MANE Select	NP_004658.3:n.11817-7_11817-6insGGGTGTGTTTGGGGGG