Canonical Allele Identifier: CA616712386
Gene: HERC2 HGNC NCBI

Linked Data

dbSNP Id: rs1566936791

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28141865_28141867del , CM000677.2:g.28141865_28141867del GRCh38
NC_000015.9:g.28387011_28387013del , CM000677.1:g.28387011_28387013del GRCh37
NC_000015.8:g.26060606_26060608del NCBI36
NG_016355.1:g.185286_185288del

Transcript Alleles

HGVS Amino-acid Change
ENST00000261609.13:c.11701-18_11701-16del MANE Select ENSP00000261609.8:n.11701-18_11701-16del
ENST00000650509.1:c.3412-18_3412-16del ENSP00000496936.1:n.3412-18_3412-16del
ENST00000261609.11:c.11701-18_11701-16del ENSP00000261609.7:n.11701-18_11701-16del
ENST00000564519.1:n.216-18_216-16del
NM_004667.5:c.11701-18_11701-16del NP_004658.3:n.11701-18_11701-16del
XM_005268276.3:c.11587-18_11587-16del XP_005268333.1:n.11587-18_11587-16del
XM_005268277.3:c.11587-18_11587-16del XP_005268334.1:n.11587-18_11587-16del
XM_006720726.2:c.11686-18_11686-16del XP_006720789.1:n.11686-18_11686-16del
XM_006720727.2:c.11443-18_11443-16del XP_006720790.1:n.11443-18_11443-16del
XM_011522131.1:c.11218-18_11218-16del XP_011520433.1:n.11218-18_11218-16del
XM_011522132.1:c.9217-18_9217-16del XP_011520434.1:n.9217-18_9217-16del
XM_011522133.1:c.8446-18_8446-16del XP_011520435.1:n.8446-18_8446-16del
XM_011522134.1:c.5818-18_5818-16del XP_011520436.1:n.5818-18_5818-16del
XM_005268276.5:c.11587-18_11587-16del XP_005268333.1:n.11587-18_11587-16del
XM_006720726.3:c.11686-18_11686-16del XP_006720789.1:n.11686-18_11686-16del
XM_006720727.3:c.11443-18_11443-16del XP_006720790.1:n.11443-18_11443-16del
XM_017022695.1:c.11587-18_11587-16del XP_016878184.1:n.11587-18_11587-16del
XM_017022696.1:c.11587-18_11587-16del XP_016878185.1:n.11587-18_11587-16del
XM_017022697.1:c.4867-18_4867-16del XP_016878186.1:n.4867-18_4867-16del
XM_017022698.1:c.4867-18_4867-16del XP_016878187.1:n.4867-18_4867-16del
NM_004667.6:c.11701-18_11701-16del MANE Select NP_004658.3:n.11701-18_11701-16del