Canonical Allele Identifier: CA655844917

Gene: HERC2

Linked Data

• COSMIC: COSN19661229

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28111732_28111733insA , CM000677.2:g.28111732_28111733insA	GRCh38
NC_000015.9:g.28356878_28356879insA , CM000677.1:g.28356878_28356879insA	GRCh37
NC_000015.8:g.26030473_26030474insA	NCBI36
NG_016355.1:g.215417_215418insT

Transcript Alleles

HGVS	Amino-acid change
ENST00000261609.13:c.*30_*31insT MANE Select	ENSP00000261609.8:n.*30_*31insT
ENST00000650509.1:c.6014_6015insT	ENSP00000496936.1:n.6014_6015insT
ENST00000261609.11:c.*30_*31insT	ENSP00000261609.7:n.*30_*31insT
ENST00000566635.5:n.1660_1661insT
NM_004667.5:c.*30_*31insT	NP_004658.3:n.*30_*31insT
XM_005268276.3:c.*30_*31insT	XP_005268333.1:n.*30_*31insT
XM_005268277.3:c.*30_*31insT	XP_005268334.1:n.*30_*31insT
XM_006720726.2:c.*30_*31insT	XP_006720789.1:n.*30_*31insT
XM_006720727.2:c.*30_*31insT	XP_006720790.1:n.*30_*31insT
XM_011522131.1:c.*30_*31insT	XP_011520433.1:n.*30_*31insT
XM_011522132.1:c.*30_*31insT	XP_011520434.1:n.*30_*31insT
XM_011522133.1:c.*30_*31insT	XP_011520435.1:n.*30_*31insT
XM_011522134.1:c.*30_*31insT	XP_011520436.1:n.*30_*31insT
XM_005268276.5:c.*30_*31insT	XP_005268333.1:n.*30_*31insT
XM_006720726.3:c.*30_*31insT	XP_006720789.1:n.*30_*31insT
XM_006720727.3:c.*30_*31insT	XP_006720790.1:n.*30_*31insT
XM_017022695.1:c.*30_*31insT	XP_016878184.1:n.*30_*31insT
XM_017022696.1:c.*30_*31insT	XP_016878185.1:n.*30_*31insT
XM_017022697.1:c.*30_*31insT	XP_016878186.1:n.*30_*31insT
XM_017022698.1:c.*30_*31insT	XP_016878187.1:n.*30_*31insT
NM_004667.6:c.*30_*31insT MANE Select	NP_004658.3:n.*30_*31insT