Canonical Allele Identifier: CA993122610

Gene: INSR

Linked Data

• dbSNP Id: rs1568489189
• gnomAD v3: 19-7211935-C-CGTTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTCCCCCATCACTGTTACCTTAAAGTAGGGTTTCTCAGCCTCAGGACTGGTGTTATTCAGAGTCGGATCTTCATCTGGGGTGGGGCT
• gnomAD v4: 19-7211935-C-CGTTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTCCCCCATCACTGTTACCTTAAAGTAGGGTTTCTCAGCCTCAGGACTGGTGTTATTCAGAGTCGGATCTTCATCTGGGGTGGGGCT

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7211990_7211991insCCTTAAAGTAGGGTTTCTCAGCCTCAGGACTGGTGTTATTCAGAGTCGGATCTTCATCTGGGGTGGGGCTGTTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTCCCCCATCACTGTTA , CM000681.2:g.7211990_7211991insCCTTAAAGTAGGGTTTCTCAGCCTCAGGACTGGTGTTATTCAGAGTCGGATCTTCATCTGGGGTGGGGCTGTTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTCCCCCATCACTGTTA	GRCh38
NC_000019.9:g.7212001_7212002insCCTTAAAGTAGGGTTTCTCAGCCTCAGGACTGGTGTTATTCAGAGTCGGATCTTCATCTGGGGTGGGGCTGTTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTCCCCCATCACTGTTA , CM000681.1:g.7212001_7212002insCCTTAAAGTAGGGTTTCTCAGCCTCAGGACTGGTGTTATTCAGAGTCGGATCTTCATCTGGGGTGGGGCTGTTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTCCCCCATCACTGTTA	GRCh37
NC_000019.8:g.7163001_7163002insCCTTAAAGTAGGGTTTCTCAGCCTCAGGACTGGTGTTATTCAGAGTCGGATCTTCATCTGGGGTGGGGCTGTTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTCCCCCATCACTGTTA	NCBI36
NG_008852.2:g.87065_87066insAGCCCCACCCCAGATGAAGATCCGACTCTGAATAACACCAGTCCTGAGGCTGAGAAACCCTACTTTAAGGTAACAGTGATGGGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-27299_653-27298insAGCCCCACCCCAGATGAAGATCCGACTCTGAATAACACCAGTCCTGAGGCTGAGAAACCCTACTTTAAGGTAACAGTGATGGGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAAC MANE Select	ENSP00000303830.4:n.653-27299_653-27298insAGCCCCACCCCAGATGAAG...
ENST00000302850.9:c.653-27299_653-27298insAGCCCCACCCCAGATGAAGATCCGACTCTGAATAACACCAGTCCTGAGGCTGAGAAACCCTACTTTAAGGTAACAGTGATGGGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAAC	ENSP00000303830.4:n.653-27299_653-27298insAGCCCCACCCCAGATGAAG...
ENST00000341500.9:c.653-27299_653-27298insAGCCCCACCCCAGATGAAGATCCGACTCTGAATAACACCAGTCCTGAGGCTGAGAAACCCTACTTTAAGGTAACAGTGATGGGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAAC	ENSP00000342838.4:n.653-27299_653-27298insAGCCCCACCCCAGATGAAG...
ENST00000598216.1:n.628-27299_628-27298insAGCCCCACCCCAGATGAAGATCCGACTCTGAATAACACCAGTCCTGAGGCTGAGAAACCCTACTTTAAGGTAACAGTGATGGGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAAC
NM_000208.2:c.653-27299_653-27298insAGCCCCACCCCAGATGAAGATCCGACTCTGAATAACACCAGTCCTGAGGCTGAGAAACCCTACTTTAAGGTAACAGTGATGGGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAAC	NP_000199.2:n.653-27299_653-27298insAGCCCCACCCCAGATGAAGATCCGA...
NM_000208.3:c.653-27299_653-27298insAGCCCCACCCCAGATGAAGATCCGACTCTGAATAACACCAGTCCTGAGGCTGAGAAACCCTACTTTAAGGTAACAGTGATGGGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAAC	NP_000199.2:n.653-27299_653-27298insAGCCCCACCCCAGATGAAGATCCGA...
NM_001079817.1:c.653-27299_653-27298insAGCCCCACCCCAGATGAAGATCCGACTCTGAATAACACCAGTCCTGAGGCTGAGAAACCCTACTTTAAGGTAACAGTGATGGGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAAC	NP_001073285.1:n.653-27299_653-27298insAGCCCCACCCCAGATGAAGATC...
NM_001079817.2:c.653-27299_653-27298insAGCCCCACCCCAGATGAAGATCCGACTCTGAATAACACCAGTCCTGAGGCTGAGAAACCCTACTTTAAGGTAACAGTGATGGGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAAC	NP_001073285.1:n.653-27299_653-27298insAGCCCCACCCCAGATGAAGATC...
XM_011527988.1:c.731-27299_731-27298insAGCCCCACCCCAGATGAAGATCCGACTCTGAATAACACCAGTCCTGAGGCTGAGAAACCCTACTTTAAGGTAACAGTGATGGGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAAC	XP_011526290.1:n.731-27299_731-27298insAGCCCCACCCCAGATGAAGATC...
XM_011527989.1:c.731-27299_731-27298insAGCCCCACCCCAGATGAAGATCCGACTCTGAATAACACCAGTCCTGAGGCTGAGAAACCCTACTTTAAGGTAACAGTGATGGGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAAC	XP_011526291.1:n.731-27299_731-27298insAGCCCCACCCCAGATGAAGATC...
XM_011527988.2:c.653-27299_653-27298insAGCCCCACCCCAGATGAAGATCCGACTCTGAATAACACCAGTCCTGAGGCTGAGAAACCCTACTTTAAGGTAACAGTGATGGGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAAC	XP_011526290.2:n.653-27299_653-27298insAGCCCCACCCCAGATGAAGATC...
XM_011527989.3:c.653-27299_653-27298insAGCCCCACCCCAGATGAAGATCCGACTCTGAATAACACCAGTCCTGAGGCTGAGAAACCCTACTTTAAGGTAACAGTGATGGGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAAC	XP_011526291.2:n.653-27299_653-27298insAGCCCCACCCCAGATGAAGATC...
NM_000208.4:c.653-27299_653-27298insAGCCCCACCCCAGATGAAGATCCGACTCTGAATAACACCAGTCCTGAGGCTGAGAAACCCTACTTTAAGGTAACAGTGATGGGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAAC MANE Select	NP_000199.2:n.653-27299_653-27298insAGCCCCACCCCAGATGAAGATCCGA...
NM_001079817.3:c.653-27299_653-27298insAGCCCCACCCCAGATGAAGATCCGACTCTGAATAACACCAGTCCTGAGGCTGAGAAACCCTACTTTAAGGTAACAGTGATGGGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAAC	NP_001073285.1:n.653-27299_653-27298insAGCCCCACCCCAGATGAAGATC...