Canonical Allele Identifier: CA2501115231
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7267633_7267634insTCGGTGTGAAAATGATGGATTGAAGCGCCATGCAAGCACCCTTATGCTGTGAAGCTGATTTAGTCTGCAAATAAGAAGCAGCCT , CM000681.2:g.7267633_7267634insTCGGTGTGAAAATGATGGATTGAAGCGCCATGCAAGCACCCTTATGCTGTGAAGCTGATTTAGTCTGCAAATAAGAAGCAGCCT GRCh38
NC_000019.9:g.7267644_7267645insTCGGTGTGAAAATGATGGATTGAAGCGCCATGCAAGCACCCTTATGCTGTGAAGCTGATTTAGTCTGCAAATAAGAAGCAGCCT , CM000681.1:g.7267644_7267645insTCGGTGTGAAAATGATGGATTGAAGCGCCATGCAAGCACCCTTATGCTGTGAAGCTGATTTAGTCTGCAAATAAGAAGCAGCCT GRCh37
NC_000019.8:g.7218644_7218645insTCGGTGTGAAAATGATGGATTGAAGCGCCATGCAAGCACCCTTATGCTGTGAAGCTGATTTAGTCTGCAAATAAGAAGCAGCCT NCBI36
NG_008852.2:g.31368_31369insGGCTGCTTCTTATTTGCAGACTAAATCAGCTTCACAGCATAAGGGTGCTTGCATGGCGCTTCAATCCATCATTTTCACACCGAA

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.364_365insGGCTGCTTCTTATTTGCAGACTAAATCAGCTTCACAGCATAAGGGTGCTTGCATGGCGCTTCAATCCATCATTTTCACACCGAA MANE Select ENSP00000303830.4:p.Val121_Ile122insArgLeuLeuLeuIleCysArgLeuA...
ENST00000302850.9:c.364_365insGGCTGCTTCTTATTTGCAGACTAAATCAGCTTCACAGCATAAGGGTGCTTGCATGGCGCTTCAATCCATCATTTTCACACCGAA ENSP00000303830.4:p.Val121_Ile122insArgLeuLeuLeuIleCysArgLeuA...
ENST00000341500.9:c.364_365insGGCTGCTTCTTATTTGCAGACTAAATCAGCTTCACAGCATAAGGGTGCTTGCATGGCGCTTCAATCCATCATTTTCACACCGAA ENSP00000342838.4:p.Val121_Ile122insArgLeuLeuLeuIleCysArgLeuA...
ENST00000598216.1:n.339_340insGGCTGCTTCTTATTTGCAGACTAAATCAGCTTCACAGCATAAGGGTGCTTGCATGGCGCTTCAATCCATCATTTTCACACCGAA
NM_000208.2:c.364_365insGGCTGCTTCTTATTTGCAGACTAAATCAGCTTCACAGCATAAGGGTGCTTGCATGGCGCTTCAATCCATCATTTTCACACCGAA NP_000199.2:p.Val121_Ile122insArgLeuLeuLeuIleCysArgLeuAsnGlnL...
NM_000208.3:c.364_365insGGCTGCTTCTTATTTGCAGACTAAATCAGCTTCACAGCATAAGGGTGCTTGCATGGCGCTTCAATCCATCATTTTCACACCGAA NP_000199.2:p.Val121_Ile122insArgLeuLeuLeuIleCysArgLeuAsnGlnL...
NM_001079817.1:c.364_365insGGCTGCTTCTTATTTGCAGACTAAATCAGCTTCACAGCATAAGGGTGCTTGCATGGCGCTTCAATCCATCATTTTCACACCGAA NP_001073285.1:p.Val121_Ile122insArgLeuLeuLeuIleCysArgLeuAsnG...
NM_001079817.2:c.364_365insGGCTGCTTCTTATTTGCAGACTAAATCAGCTTCACAGCATAAGGGTGCTTGCATGGCGCTTCAATCCATCATTTTCACACCGAA NP_001073285.1:p.Val121_Ile122insArgLeuLeuLeuIleCysArgLeuAsnG...
XM_011527988.1:c.442_443insGGCTGCTTCTTATTTGCAGACTAAATCAGCTTCACAGCATAAGGGTGCTTGCATGGCGCTTCAATCCATCATTTTCACACCGAA XP_011526290.1:p.Val147_Ile148insArgLeuLeuLeuIleCysArgLeuAsnG...
XM_011527989.1:c.442_443insGGCTGCTTCTTATTTGCAGACTAAATCAGCTTCACAGCATAAGGGTGCTTGCATGGCGCTTCAATCCATCATTTTCACACCGAA XP_011526291.1:p.Val147_Ile148insArgLeuLeuLeuIleCysArgLeuAsnG...
XM_011527988.2:c.364_365insGGCTGCTTCTTATTTGCAGACTAAATCAGCTTCACAGCATAAGGGTGCTTGCATGGCGCTTCAATCCATCATTTTCACACCGAA XP_011526290.2:p.Val121_Ile122insArgLeuLeuLeuIleCysArgLeuAsnG...
XM_011527989.3:c.364_365insGGCTGCTTCTTATTTGCAGACTAAATCAGCTTCACAGCATAAGGGTGCTTGCATGGCGCTTCAATCCATCATTTTCACACCGAA XP_011526291.2:p.Val121_Ile122insArgLeuLeuLeuIleCysArgLeuAsnG...
NM_000208.4:c.364_365insGGCTGCTTCTTATTTGCAGACTAAATCAGCTTCACAGCATAAGGGTGCTTGCATGGCGCTTCAATCCATCATTTTCACACCGAA MANE Select NP_000199.2:p.Val121_Ile122insArgLeuLeuLeuIleCysArgLeuAsnGlnL...
NM_001079817.3:c.364_365insGGCTGCTTCTTATTTGCAGACTAAATCAGCTTCACAGCATAAGGGTGCTTGCATGGCGCTTCAATCCATCATTTTCACACCGAA NP_001073285.1:p.Val121_Ile122insArgLeuLeuLeuIleCysArgLeuAsnG...