Canonical Allele Identifier: CA2166520843

Gene: HERC2

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28208203_28208208delinsCCTCTT , CM000677.2:g.28208203_28208208delinsCCTCTT	GRCh38
NC_000015.9:g.28453349_28453354delinsCCTCTT , CM000677.1:g.28453349_28453354delinsCCTCTT	GRCh37
NC_000015.8:g.26126944_26126949delinsCCTCTT	NCBI36
NG_016355.1:g.118942_118947delinsAAGAGG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.7070-1826_7070-1821delinsAAGAGG MANE Select	ENSP00000261609.8:n.7070-1826_7070-1821delinsAAGAGG
ENST00000261609.11:c.7070-1826_7070-1821delinsAAGAGG	ENSP00000261609.7:n.7070-1826_7070-1821delinsAAGAGG
NM_004667.5:c.7070-1826_7070-1821delinsAAGAGG	NP_004658.3:n.7070-1826_7070-1821delinsAAGAGG
XM_005268276.3:c.6956-1826_6956-1821delinsAAGAGG	XP_005268333.1:n.6956-1826_6956-1821delinsAAGAGG
XM_005268277.3:c.6956-1826_6956-1821delinsAAGAGG	XP_005268334.1:n.6956-1826_6956-1821delinsAAGAGG
XM_006720726.2:c.7055-1826_7055-1821delinsAAGAGG	XP_006720789.1:n.7055-1826_7055-1821delinsAAGAGG
XM_006720727.2:c.6812-1826_6812-1821delinsAAGAGG	XP_006720790.1:n.6812-1826_6812-1821delinsAAGAGG
XM_011522131.1:c.6587-1826_6587-1821delinsAAGAGG	XP_011520433.1:n.6587-1826_6587-1821delinsAAGAGG
XM_011522132.1:c.4586-1826_4586-1821delinsAAGAGG	XP_011520434.1:n.4586-1826_4586-1821delinsAAGAGG
XM_011522133.1:c.3815-1826_3815-1821delinsAAGAGG	XP_011520435.1:n.3815-1826_3815-1821delinsAAGAGG
XM_011522134.1:c.1187-1826_1187-1821delinsAAGAGG	XP_011520436.1:n.1187-1826_1187-1821delinsAAGAGG
XM_011522135.1:c.7070-1826_7070-1821delinsAAGAGG	XP_011520437.1:n.7070-1826_7070-1821delinsAAGAGG
XM_011522136.1:c.7070-1826_7070-1821delinsAAGAGG	XP_011520438.1:n.7070-1826_7070-1821delinsAAGAGG
XM_011522137.1:c.7070-1826_7070-1821delinsAAGAGG	XP_011520439.1:n.7070-1826_7070-1821delinsAAGAGG
XR_931930.1:n.7199-1826_7199-1821delinsAAGAGG
XR_931931.1:n.7199-1826_7199-1821delinsAAGAGG
XM_005268276.5:c.6956-1826_6956-1821delinsAAGAGG	XP_005268333.1:n.6956-1826_6956-1821delinsAAGAGG
XM_006720726.3:c.7055-1826_7055-1821delinsAAGAGG	XP_006720789.1:n.7055-1826_7055-1821delinsAAGAGG
XM_006720727.3:c.6812-1826_6812-1821delinsAAGAGG	XP_006720790.1:n.6812-1826_6812-1821delinsAAGAGG
XM_017022695.1:c.6956-1826_6956-1821delinsAAGAGG	XP_016878184.1:n.6956-1826_6956-1821delinsAAGAGG
XM_017022696.1:c.6956-1826_6956-1821delinsAAGAGG	XP_016878185.1:n.6956-1826_6956-1821delinsAAGAGG
XM_017022697.1:c.236-1826_236-1821delinsAAGAGG	XP_016878186.1:n.236-1826_236-1821delinsAAGAGG
XM_017022698.1:c.236-1826_236-1821delinsAAGAGG	XP_016878187.1:n.236-1826_236-1821delinsAAGAGG
XR_001751410.1:n.7200-1826_7200-1821delinsAAGAGG
XR_931930.2:n.7200-1826_7200-1821delinsAAGAGG
NM_004667.6:c.7070-1826_7070-1821delinsAAGAGG MANE Select	NP_004658.3:n.7070-1826_7070-1821delinsAAGAGG