Canonical Allele Identifier: CA968037924

Gene: HERC2

Linked Data

• gnomAD v3: 15-28208072-C-CG
• gnomAD v4: 15-28208072-C-CG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28208072_28208073insG , CM000677.2:g.28208072_28208073insG	GRCh38
NC_000015.9:g.28453218_28453219insG , CM000677.1:g.28453218_28453219insG	GRCh37
NC_000015.8:g.26126813_26126814insG	NCBI36
NG_016355.1:g.119077_119078insC

Transcript Alleles

HGVS	Amino-acid change
ENST00000261609.13:c.7070-1691_7070-1690insC MANE Select	ENSP00000261609.8:n.7070-1691_7070-1690in...
ENST00000261609.11:c.7070-1691_7070-1690insC	ENSP00000261609.7:n.7070-1691_7070-1690in...
NM_004667.5:c.7070-1691_7070-1690insC	NP_004658.3:n.7070-1691_7070-1690insC
XM_005268276.3:c.6956-1691_6956-1690insC	XP_005268333.1:n.6956-1691_6956-1690insC
XM_005268277.3:c.6956-1691_6956-1690insC	XP_005268334.1:n.6956-1691_6956-1690insC
XM_006720726.2:c.7055-1691_7055-1690insC	XP_006720789.1:n.7055-1691_7055-1690insC
XM_006720727.2:c.6812-1691_6812-1690insC	XP_006720790.1:n.6812-1691_6812-1690insC
XM_011522131.1:c.6587-1691_6587-1690insC	XP_011520433.1:n.6587-1691_6587-1690insC
XM_011522132.1:c.4586-1691_4586-1690insC	XP_011520434.1:n.4586-1691_4586-1690insC
XM_011522133.1:c.3815-1691_3815-1690insC	XP_011520435.1:n.3815-1691_3815-1690insC
XM_011522134.1:c.1187-1691_1187-1690insC	XP_011520436.1:n.1187-1691_1187-1690insC
XM_011522135.1:c.7070-1691_7070-1690insC	XP_011520437.1:n.7070-1691_7070-1690insC
XM_011522136.1:c.7070-1691_7070-1690insC	XP_011520438.1:n.7070-1691_7070-1690insC
XM_011522137.1:c.7070-1691_7070-1690insC	XP_011520439.1:n.7070-1691_7070-1690insC
XR_931930.1:n.7199-1691_7199-1690insC
XR_931931.1:n.7199-1691_7199-1690insC
XM_005268276.5:c.6956-1691_6956-1690insC	XP_005268333.1:n.6956-1691_6956-1690insC
XM_006720726.3:c.7055-1691_7055-1690insC	XP_006720789.1:n.7055-1691_7055-1690insC
XM_006720727.3:c.6812-1691_6812-1690insC	XP_006720790.1:n.6812-1691_6812-1690insC
XM_017022695.1:c.6956-1691_6956-1690insC	XP_016878184.1:n.6956-1691_6956-1690insC
XM_017022696.1:c.6956-1691_6956-1690insC	XP_016878185.1:n.6956-1691_6956-1690insC
XM_017022697.1:c.236-1691_236-1690insC	XP_016878186.1:n.236-1691_236-1690insC
XM_017022698.1:c.236-1691_236-1690insC	XP_016878187.1:n.236-1691_236-1690insC
XR_001751410.1:n.7200-1691_7200-1690insC
XR_931930.2:n.7200-1691_7200-1690insC
NM_004667.6:c.7070-1691_7070-1690insC MANE Select	NP_004658.3:n.7070-1691_7070-1690insC