Canonical Allele Identifier: CA2166491684

Gene: HERC2

Linked Data

• dbSNP Id: rs1840625758

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28182977_28182980del , CM000677.2:g.28182977_28182980del	GRCh38
NC_000015.9:g.28428123_28428126del , CM000677.1:g.28428123_28428126del	GRCh37
NC_000015.8:g.26101718_26101721del	NCBI36
NG_016355.1:g.144174_144177del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.8826-464_8826-461del MANE Select	ENSP00000261609.8:n.8826-464_8826-461del
ENST00000650509.1:c.537-464_537-461del	ENSP00000496936.1:n.537-464_537-461del
ENST00000261609.11:c.8826-464_8826-461del	ENSP00000261609.7:n.8826-464_8826-461del
NM_004667.5:c.8826-464_8826-461del	NP_004658.3:n.8826-464_8826-461del
XM_005268276.3:c.8712-464_8712-461del	XP_005268333.1:n.8712-464_8712-461del
XM_005268277.3:c.8712-464_8712-461del	XP_005268334.1:n.8712-464_8712-461del
XM_006720726.2:c.8811-464_8811-461del	XP_006720789.1:n.8811-464_8811-461del
XM_006720727.2:c.8568-464_8568-461del	XP_006720790.1:n.8568-464_8568-461del
XM_011522131.1:c.8343-464_8343-461del	XP_011520433.1:n.8343-464_8343-461del
XM_011522132.1:c.6342-464_6342-461del	XP_011520434.1:n.6342-464_6342-461del
XM_011522133.1:c.5571-464_5571-461del	XP_011520435.1:n.5571-464_5571-461del
XM_011522134.1:c.2943-464_2943-461del	XP_011520436.1:n.2943-464_2943-461del
XR_931930.1:n.8955-464_8955-461del
XM_005268276.5:c.8712-464_8712-461del	XP_005268333.1:n.8712-464_8712-461del
XM_006720726.3:c.8811-464_8811-461del	XP_006720789.1:n.8811-464_8811-461del
XM_006720727.3:c.8568-464_8568-461del	XP_006720790.1:n.8568-464_8568-461del
XM_017022695.1:c.8712-464_8712-461del	XP_016878184.1:n.8712-464_8712-461del
XM_017022696.1:c.8712-464_8712-461del	XP_016878185.1:n.8712-464_8712-461del
XM_017022697.1:c.1992-464_1992-461del	XP_016878186.1:n.1992-464_1992-461del
XM_017022698.1:c.1992-464_1992-461del	XP_016878187.1:n.1992-464_1992-461del
XR_931930.2:n.8956-464_8956-461del
NM_004667.6:c.8826-464_8826-461del MANE Select	NP_004658.3:n.8826-464_8826-461del