Canonical Allele Identifier: CA645613083

Gene: INSR

Linked Data

• COSMIC: COSM5347392 ; COSM5347393

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117345_7117363del , CM000681.2:g.7117345_7117363del	GRCh38
NC_000019.9:g.7117356_7117374del , CM000681.1:g.7117356_7117374del	GRCh37
NC_000019.8:g.7068356_7068374del	NCBI36
NG_008852.2:g.181644_181662del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3848_3866del MANE Select	ENSP00000303830.4:p.Phe1283CysfsTer?
ENST00000302850.9:c.3848_3866del	ENSP00000303830.4:p.Phe1283CysfsTer?
ENST00000341500.9:c.3812_3830del	ENSP00000342838.4:p.Phe1271CysfsTer?
NM_000208.2:c.3848_3866del	NP_000199.2:p.Phe1283CysfsTer?
NM_000208.3:c.3848_3866del	NP_000199.2:p.Phe1283CysfsTer?
NM_001079817.1:c.3812_3830del	NP_001073285.1:p.Phe1271CysfsTer?
NM_001079817.2:c.3812_3830del	NP_001073285.1:p.Phe1271CysfsTer?
XM_011527988.1:c.3923_3941del	XP_011526290.1:p.Phe1308CysfsTer?
XM_011527989.1:c.3887_3905del	XP_011526291.1:p.Phe1296CysfsTer?
XM_011527988.2:c.3845_3863del	XP_011526290.2:p.Phe1282CysfsTer?
XM_011527989.3:c.3809_3827del	XP_011526291.2:p.Phe1270CysfsTer?
NM_000208.4:c.3848_3866del MANE Select	NP_000199.2:p.Phe1283CysfsTer?
NM_001079817.3:c.3812_3830del	NP_001073285.1:p.Phe1271CysfsTer?