Canonical Allele Identifier: CA968039588

Gene: HERC2

Linked Data

• gnomAD v3: 15-28111740-T-TTAAAAAA
• gnomAD v4: 15-28111740-T-TTAAAAAA

Genomic Alleles

HGVS	Genome Assembly
NC_000015.10:g.28111740_28111741insTAAAAAA , CM000677.2:g.28111740_28111741insTAAAAAA	GRCh38
NC_000015.9:g.28356886_28356887insTAAAAAA , CM000677.1:g.28356886_28356887insTAAAAAA	GRCh37
NC_000015.8:g.26030481_26030482insTAAAAAA	NCBI36
NG_016355.1:g.215409_215410insTTTTTTA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000261609.13:c.*22_*23insTTTTTTA MANE Select	ENSP00000261609.8:n.*22_*23insTTTTTTA
ENST00000650509.1:c.6006_6007insTTTTTTA	ENSP00000496936.1:n.6006_6007insTTTTTTA
ENST00000261609.11:c.*22_*23insTTTTTTA	ENSP00000261609.7:n.*22_*23insTTTTTTA
ENST00000566635.5:n.1652_1653insTTTTTTA
NM_004667.5:c.*22_*23insTTTTTTA	NP_004658.3:n.*22_*23insTTTTTTA
XM_005268276.3:c.*22_*23insTTTTTTA	XP_005268333.1:n.*22_*23insTTTTTTA
XM_005268277.3:c.*22_*23insTTTTTTA	XP_005268334.1:n.*22_*23insTTTTTTA
XM_006720726.2:c.*22_*23insTTTTTTA	XP_006720789.1:n.*22_*23insTTTTTTA
XM_006720727.2:c.*22_*23insTTTTTTA	XP_006720790.1:n.*22_*23insTTTTTTA
XM_011522131.1:c.*22_*23insTTTTTTA	XP_011520433.1:n.*22_*23insTTTTTTA
XM_011522132.1:c.*22_*23insTTTTTTA	XP_011520434.1:n.*22_*23insTTTTTTA
XM_011522133.1:c.*22_*23insTTTTTTA	XP_011520435.1:n.*22_*23insTTTTTTA
XM_011522134.1:c.*22_*23insTTTTTTA	XP_011520436.1:n.*22_*23insTTTTTTA
XM_005268276.5:c.*22_*23insTTTTTTA	XP_005268333.1:n.*22_*23insTTTTTTA
XM_006720726.3:c.*22_*23insTTTTTTA	XP_006720789.1:n.*22_*23insTTTTTTA
XM_006720727.3:c.*22_*23insTTTTTTA	XP_006720790.1:n.*22_*23insTTTTTTA
XM_017022695.1:c.*22_*23insTTTTTTA	XP_016878184.1:n.*22_*23insTTTTTTA
XM_017022696.1:c.*22_*23insTTTTTTA	XP_016878185.1:n.*22_*23insTTTTTTA
XM_017022697.1:c.*22_*23insTTTTTTA	XP_016878186.1:n.*22_*23insTTTTTTA
XM_017022698.1:c.*22_*23insTTTTTTA	XP_016878187.1:n.*22_*23insTTTTTTA
NM_004667.6:c.*22_*23insTTTTTTA MANE Select	NP_004658.3:n.*22_*23insTTTTTTA