Canonical Allele Identifier: CA968039579

Gene: HERC2

Linked Data

• dbSNP Id: rs1887665732

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28111732_28111739del , CM000677.2:g.28111732_28111739del	GRCh38
NC_000015.9:g.28356878_28356885del , CM000677.1:g.28356878_28356885del	GRCh37
NC_000015.8:g.26030473_26030480del	NCBI36
NG_016355.1:g.215415_215422del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.*28_*35del MANE Select	ENSP00000261609.8:n.*28_*35del
ENST00000650509.1:c.6012_6019del	ENSP00000496936.1:n.6012_6019del
ENST00000261609.11:c.*28_*35del	ENSP00000261609.7:n.*28_*35del
ENST00000566635.5:n.1658_1665del
NM_004667.5:c.*28_*35del	NP_004658.3:n.*28_*35del
XM_005268276.3:c.*28_*35del	XP_005268333.1:n.*28_*35del
XM_005268277.3:c.*28_*35del	XP_005268334.1:n.*28_*35del
XM_006720726.2:c.*28_*35del	XP_006720789.1:n.*28_*35del
XM_006720727.2:c.*28_*35del	XP_006720790.1:n.*28_*35del
XM_011522131.1:c.*28_*35del	XP_011520433.1:n.*28_*35del
XM_011522132.1:c.*28_*35del	XP_011520434.1:n.*28_*35del
XM_011522133.1:c.*28_*35del	XP_011520435.1:n.*28_*35del
XM_011522134.1:c.*28_*35del	XP_011520436.1:n.*28_*35del
XM_005268276.5:c.*28_*35del	XP_005268333.1:n.*28_*35del
XM_006720726.3:c.*28_*35del	XP_006720789.1:n.*28_*35del
XM_006720727.3:c.*28_*35del	XP_006720790.1:n.*28_*35del
XM_017022695.1:c.*28_*35del	XP_016878184.1:n.*28_*35del
XM_017022696.1:c.*28_*35del	XP_016878185.1:n.*28_*35del
XM_017022697.1:c.*28_*35del	XP_016878186.1:n.*28_*35del
XM_017022698.1:c.*28_*35del	XP_016878187.1:n.*28_*35del
NM_004667.6:c.*28_*35del MANE Select	NP_004658.3:n.*28_*35del