Canonical Allele Identifier: CA2813449715
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7117163del , CM000681.2:g.7117163del GRCh38
NC_000019.9:g.7117174del , CM000681.1:g.7117174del GRCh37
NC_000019.8:g.7068174del NCBI36
NG_008852.2:g.181838del

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.4042del MANE Select ENSP00000303830.4:p.Ser1348ArgfsTer17
ENST00000302850.9:c.4042del ENSP00000303830.4:p.Ser1348ArgfsTer17
ENST00000341500.9:c.4006del ENSP00000342838.4:p.Ser1336ArgfsTer17
NM_000208.2:c.4042del NP_000199.2:p.Ser1348ArgfsTer17
NM_000208.3:c.4042del NP_000199.2:p.Ser1348ArgfsTer17
NM_001079817.1:c.4006del NP_001073285.1:p.Ser1336ArgfsTer17
NM_001079817.2:c.4006del NP_001073285.1:p.Ser1336ArgfsTer17
XM_011527988.1:c.4117del XP_011526290.1:p.Ser1373ArgfsTer17
XM_011527989.1:c.4081del XP_011526291.1:p.Ser1361ArgfsTer17
XM_011527988.2:c.4039del XP_011526290.2:p.Ser1347ArgfsTer17
XM_011527989.3:c.4003del XP_011526291.2:p.Ser1335ArgfsTer17
NM_000208.4:c.4042del MANE Select NP_000199.2:p.Ser1348ArgfsTer17
NM_001079817.3:c.4006del NP_001073285.1:p.Ser1336ArgfsTer17