Canonical Allele Identifier: CA2166480130

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141861_28141864delinsTATG , CM000677.2:g.28141861_28141864delinsTATG	GRCh38
NC_000015.9:g.28387007_28387010delinsTATG , CM000677.1:g.28387007_28387010delinsTATG	GRCh37
NC_000015.8:g.26060602_26060605delinsTATG	NCBI36
NG_016355.1:g.185286_185289delinsCATA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11701-18_11701-15delinsCATA MANE Select	ENSP00000261609.8:n.11701-18_11701-15delinsCATA
ENST00000650509.1:c.3412-18_3412-15delinsCATA	ENSP00000496936.1:n.3412-18_3412-15delinsCATA
ENST00000261609.11:c.11701-18_11701-15delinsCATA	ENSP00000261609.7:n.11701-18_11701-15delinsCATA
ENST00000564519.1:n.216-18_216-15delinsCATA
NM_004667.5:c.11701-18_11701-15delinsCATA	NP_004658.3:n.11701-18_11701-15delinsCATA
XM_005268276.3:c.11587-18_11587-15delinsCATA	XP_005268333.1:n.11587-18_11587-15delinsCATA
XM_005268277.3:c.11587-18_11587-15delinsCATA	XP_005268334.1:n.11587-18_11587-15delinsCATA
XM_006720726.2:c.11686-18_11686-15delinsCATA	XP_006720789.1:n.11686-18_11686-15delinsCATA
XM_006720727.2:c.11443-18_11443-15delinsCATA	XP_006720790.1:n.11443-18_11443-15delinsCATA
XM_011522131.1:c.11218-18_11218-15delinsCATA	XP_011520433.1:n.11218-18_11218-15delinsCATA
XM_011522132.1:c.9217-18_9217-15delinsCATA	XP_011520434.1:n.9217-18_9217-15delinsCATA
XM_011522133.1:c.8446-18_8446-15delinsCATA	XP_011520435.1:n.8446-18_8446-15delinsCATA
XM_011522134.1:c.5818-18_5818-15delinsCATA	XP_011520436.1:n.5818-18_5818-15delinsCATA
XM_005268276.5:c.11587-18_11587-15delinsCATA	XP_005268333.1:n.11587-18_11587-15delinsCATA
XM_006720726.3:c.11686-18_11686-15delinsCATA	XP_006720789.1:n.11686-18_11686-15delinsCATA
XM_006720727.3:c.11443-18_11443-15delinsCATA	XP_006720790.1:n.11443-18_11443-15delinsCATA
XM_017022695.1:c.11587-18_11587-15delinsCATA	XP_016878184.1:n.11587-18_11587-15delinsCATA
XM_017022696.1:c.11587-18_11587-15delinsCATA	XP_016878185.1:n.11587-18_11587-15delinsCATA
XM_017022697.1:c.4867-18_4867-15delinsCATA	XP_016878186.1:n.4867-18_4867-15delinsCATA
XM_017022698.1:c.4867-18_4867-15delinsCATA	XP_016878187.1:n.4867-18_4867-15delinsCATA
NM_004667.6:c.11701-18_11701-15delinsCATA MANE Select	NP_004658.3:n.11701-18_11701-15delinsCATA