Canonical Allele Identifier: CA968037909
Gene: HERC2 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000015.10:g.28208061_28208062insTTTTTT , CM000677.2:g.28208061_28208062insTTTTTT GRCh38
NC_000015.9:g.28453207_28453208insTTTTTT , CM000677.1:g.28453207_28453208insTTTTTT GRCh37
NC_000015.8:g.26126802_26126803insTTTTTT NCBI36
NG_016355.1:g.119088_119089insAAAAAA

Transcript Alleles

HGVS Amino-acid change
ENST00000261609.13:c.7070-1680_7070-1679insAAAAAA MANE Select ENSP00000261609.8:n.7070-1680_7070-1679in...
ENST00000261609.11:c.7070-1680_7070-1679insAAAAAA ENSP00000261609.7:n.7070-1680_7070-1679in...
NM_004667.5:c.7070-1680_7070-1679insAAAAAA NP_004658.3:n.7070-1680_7070-1679insAAAAA...
XM_005268276.3:c.6956-1680_6956-1679insAAAAAA XP_005268333.1:n.6956-1680_6956-1679insAA...
XM_005268277.3:c.6956-1680_6956-1679insAAAAAA XP_005268334.1:n.6956-1680_6956-1679insAA...
XM_006720726.2:c.7055-1680_7055-1679insAAAAAA XP_006720789.1:n.7055-1680_7055-1679insAA...
XM_006720727.2:c.6812-1680_6812-1679insAAAAAA XP_006720790.1:n.6812-1680_6812-1679insAA...
XM_011522131.1:c.6587-1680_6587-1679insAAAAAA XP_011520433.1:n.6587-1680_6587-1679insAA...
XM_011522132.1:c.4586-1680_4586-1679insAAAAAA XP_011520434.1:n.4586-1680_4586-1679insAA...
XM_011522133.1:c.3815-1680_3815-1679insAAAAAA XP_011520435.1:n.3815-1680_3815-1679insAA...
XM_011522134.1:c.1187-1680_1187-1679insAAAAAA XP_011520436.1:n.1187-1680_1187-1679insAA...
XM_011522135.1:c.7070-1680_7070-1679insAAAAAA XP_011520437.1:n.7070-1680_7070-1679insAA...
XM_011522136.1:c.7070-1680_7070-1679insAAAAAA XP_011520438.1:n.7070-1680_7070-1679insAA...
XM_011522137.1:c.7070-1680_7070-1679insAAAAAA XP_011520439.1:n.7070-1680_7070-1679insAA...
XR_931930.1:n.7199-1680_7199-1679insAAAAAA
XR_931931.1:n.7199-1680_7199-1679insAAAAAA
XM_005268276.5:c.6956-1680_6956-1679insAAAAAA XP_005268333.1:n.6956-1680_6956-1679insAA...
XM_006720726.3:c.7055-1680_7055-1679insAAAAAA XP_006720789.1:n.7055-1680_7055-1679insAA...
XM_006720727.3:c.6812-1680_6812-1679insAAAAAA XP_006720790.1:n.6812-1680_6812-1679insAA...
XM_017022695.1:c.6956-1680_6956-1679insAAAAAA XP_016878184.1:n.6956-1680_6956-1679insAA...
XM_017022696.1:c.6956-1680_6956-1679insAAAAAA XP_016878185.1:n.6956-1680_6956-1679insAA...
XM_017022697.1:c.236-1680_236-1679insAAAAAA XP_016878186.1:n.236-1680_236-1679insAAAA...
XM_017022698.1:c.236-1680_236-1679insAAAAAA XP_016878187.1:n.236-1680_236-1679insAAAA...
XR_001751410.1:n.7200-1680_7200-1679insAAAAAA
XR_931930.2:n.7200-1680_7200-1679insAAAAAA
NM_004667.6:c.7070-1680_7070-1679insAAAAAA MANE Select NP_004658.3:n.7070-1680_7070-1679insAAAAA...