Canonical Allele Identifier: CA2166480124

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141849_28141852delinsAAAC , CM000677.2:g.28141849_28141852delinsAAAC	GRCh38
NC_000015.9:g.28386995_28386998delinsAAAC , CM000677.1:g.28386995_28386998delinsAAAC	GRCh37
NC_000015.8:g.26060590_26060593delinsAAAC	NCBI36
NG_016355.1:g.185298_185301delinsGTTT

Transcript Alleles

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