Canonical Allele Identifier: CA2627386278

Gene: HERC2

Linked Data

• gnomAD v4: 15-28141788-TCATGCAGAA-T

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28141792_28141800del , CM000677.2:g.28141792_28141800del	GRCh38
NC_000015.9:g.28386938_28386946del , CM000677.1:g.28386938_28386946del	GRCh37
NC_000015.8:g.26060533_26060541del	NCBI36
NG_016355.1:g.185353_185361del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.11750_11758del MANE Select	ENSP00000261609.8:p.Val3917_His3919del
ENST00000650509.1:c.3461_3469del	ENSP00000496936.1:p.Val1154_His1156del
ENST00000261609.11:c.11750_11758del	ENSP00000261609.7:p.Val3917_His3919del
ENST00000564519.1:n.265_273del
NM_004667.5:c.11750_11758del	NP_004658.3:p.Val3917_His3919del
XM_005268276.3:c.11636_11644del	XP_005268333.1:p.Val3879_His3881del
XM_005268277.3:c.11636_11644del	XP_005268334.1:p.Val3879_His3881del
XM_006720726.2:c.11735_11743del	XP_006720789.1:p.Val3912_His3914del
XM_006720727.2:c.11492_11500del	XP_006720790.1:p.Val3831_His3833del
XM_011522131.1:c.11267_11275del	XP_011520433.1:p.Val3756_His3758del
XM_011522132.1:c.9266_9274del	XP_011520434.1:p.Val3089_His3091del
XM_011522133.1:c.8495_8503del	XP_011520435.1:p.Val2832_His2834del
XM_011522134.1:c.5867_5875del	XP_011520436.1:p.Val1956_His1958del
XM_005268276.5:c.11636_11644del	XP_005268333.1:p.Val3879_His3881del
XM_006720726.3:c.11735_11743del	XP_006720789.1:p.Val3912_His3914del
XM_006720727.3:c.11492_11500del	XP_006720790.1:p.Val3831_His3833del
XM_017022695.1:c.11636_11644del	XP_016878184.1:p.Val3879_His3881del
XM_017022696.1:c.11636_11644del	XP_016878185.1:p.Val3879_His3881del
XM_017022697.1:c.4916_4924del	XP_016878186.1:p.Val1639_His1641del
XM_017022698.1:c.4916_4924del	XP_016878187.1:p.Val1639_His1641del
NM_004667.6:c.11750_11758del MANE Select	NP_004658.3:p.Val3917_His3919del