Canonical Allele Identifier: CA2803510929

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141850_28141851insCCCAAACACACCCAAC , CM000677.2:g.28141850_28141851insCCCAAACACACCCAAC	GRCh38
NC_000015.9:g.28386996_28386997insCCCAAACACACCCAAC , CM000677.1:g.28386996_28386997insCCCAAACACACCCAAC	GRCh37
NC_000015.8:g.26060591_26060592insCCCAAACACACCCAAC	NCBI36
NG_016355.1:g.185299_185300insGTTGGGTGTGTTTGGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11701-5_11701-4insGTTGGGTGTGTTTGGG MANE Select	ENSP00000261609.8:n.11701-5_11701-4insGTTGGGTGTGTTTGGG
ENST00000650509.1:c.3412-5_3412-4insGTTGGGTGTGTTTGGG	ENSP00000496936.1:n.3412-5_3412-4insGTTGGGTGTGTTTGGG
ENST00000261609.11:c.11701-5_11701-4insGTTGGGTGTGTTTGGG	ENSP00000261609.7:n.11701-5_11701-4insGTTGGGTGTGTTTGGG
ENST00000564519.1:n.216-5_216-4insGTTGGGTGTGTTTGGG
NM_004667.5:c.11701-5_11701-4insGTTGGGTGTGTTTGGG	NP_004658.3:n.11701-5_11701-4insGTTGGGTGTGTTTGGG
XM_005268276.3:c.11587-5_11587-4insGTTGGGTGTGTTTGGG	XP_005268333.1:n.11587-5_11587-4insGTTGGGTGTGTTTGGG
XM_005268277.3:c.11587-5_11587-4insGTTGGGTGTGTTTGGG	XP_005268334.1:n.11587-5_11587-4insGTTGGGTGTGTTTGGG
XM_006720726.2:c.11686-5_11686-4insGTTGGGTGTGTTTGGG	XP_006720789.1:n.11686-5_11686-4insGTTGGGTGTGTTTGGG
XM_006720727.2:c.11443-5_11443-4insGTTGGGTGTGTTTGGG	XP_006720790.1:n.11443-5_11443-4insGTTGGGTGTGTTTGGG
XM_011522131.1:c.11218-5_11218-4insGTTGGGTGTGTTTGGG	XP_011520433.1:n.11218-5_11218-4insGTTGGGTGTGTTTGGG
XM_011522132.1:c.9217-5_9217-4insGTTGGGTGTGTTTGGG	XP_011520434.1:n.9217-5_9217-4insGTTGGGTGTGTTTGGG
XM_011522133.1:c.8446-5_8446-4insGTTGGGTGTGTTTGGG	XP_011520435.1:n.8446-5_8446-4insGTTGGGTGTGTTTGGG
XM_011522134.1:c.5818-5_5818-4insGTTGGGTGTGTTTGGG	XP_011520436.1:n.5818-5_5818-4insGTTGGGTGTGTTTGGG
XM_005268276.5:c.11587-5_11587-4insGTTGGGTGTGTTTGGG	XP_005268333.1:n.11587-5_11587-4insGTTGGGTGTGTTTGGG
XM_006720726.3:c.11686-5_11686-4insGTTGGGTGTGTTTGGG	XP_006720789.1:n.11686-5_11686-4insGTTGGGTGTGTTTGGG
XM_006720727.3:c.11443-5_11443-4insGTTGGGTGTGTTTGGG	XP_006720790.1:n.11443-5_11443-4insGTTGGGTGTGTTTGGG
XM_017022695.1:c.11587-5_11587-4insGTTGGGTGTGTTTGGG	XP_016878184.1:n.11587-5_11587-4insGTTGGGTGTGTTTGGG
XM_017022696.1:c.11587-5_11587-4insGTTGGGTGTGTTTGGG	XP_016878185.1:n.11587-5_11587-4insGTTGGGTGTGTTTGGG
XM_017022697.1:c.4867-5_4867-4insGTTGGGTGTGTTTGGG	XP_016878186.1:n.4867-5_4867-4insGTTGGGTGTGTTTGGG
XM_017022698.1:c.4867-5_4867-4insGTTGGGTGTGTTTGGG	XP_016878187.1:n.4867-5_4867-4insGTTGGGTGTGTTTGGG
NM_004667.6:c.11701-5_11701-4insGTTGGGTGTGTTTGGG MANE Select	NP_004658.3:n.11701-5_11701-4insGTTGGGTGTGTTTGGG