Canonical Allele Identifier: CA968039584

Gene: HERC2

Linked Data

• gnomAD v3: 15-28111734-C-CCG
• gnomAD v4: 15-28111734-C-CCG

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28111734_28111735insCG , CM000677.2:g.28111734_28111735insCG	GRCh38
NC_000015.9:g.28356880_28356881insCG , CM000677.1:g.28356880_28356881insCG	GRCh37
NC_000015.8:g.26030475_26030476insCG	NCBI36
NG_016355.1:g.215415_215416insCG

Transcript Alleles

HGVS	Amino-acid change
ENST00000261609.13:c.*28_*29insCG MANE Select	ENSP00000261609.8:n.*28_*29insCG
ENST00000650509.1:c.6012_6013insCG	ENSP00000496936.1:n.6012_6013insCG
ENST00000261609.11:c.*28_*29insCG	ENSP00000261609.7:n.*28_*29insCG
ENST00000566635.5:n.1658_1659insCG
NM_004667.5:c.*28_*29insCG	NP_004658.3:n.*28_*29insCG
XM_005268276.3:c.*28_*29insCG	XP_005268333.1:n.*28_*29insCG
XM_005268277.3:c.*28_*29insCG	XP_005268334.1:n.*28_*29insCG
XM_006720726.2:c.*28_*29insCG	XP_006720789.1:n.*28_*29insCG
XM_006720727.2:c.*28_*29insCG	XP_006720790.1:n.*28_*29insCG
XM_011522131.1:c.*28_*29insCG	XP_011520433.1:n.*28_*29insCG
XM_011522132.1:c.*28_*29insCG	XP_011520434.1:n.*28_*29insCG
XM_011522133.1:c.*28_*29insCG	XP_011520435.1:n.*28_*29insCG
XM_011522134.1:c.*28_*29insCG	XP_011520436.1:n.*28_*29insCG
XM_005268276.5:c.*28_*29insCG	XP_005268333.1:n.*28_*29insCG
XM_006720726.3:c.*28_*29insCG	XP_006720789.1:n.*28_*29insCG
XM_006720727.3:c.*28_*29insCG	XP_006720790.1:n.*28_*29insCG
XM_017022695.1:c.*28_*29insCG	XP_016878184.1:n.*28_*29insCG
XM_017022696.1:c.*28_*29insCG	XP_016878185.1:n.*28_*29insCG
XM_017022697.1:c.*28_*29insCG	XP_016878186.1:n.*28_*29insCG
XM_017022698.1:c.*28_*29insCG	XP_016878187.1:n.*28_*29insCG
NM_004667.6:c.*28_*29insCG MANE Select	NP_004658.3:n.*28_*29insCG