Canonical Allele Identifier: CA993122771

Gene: INSR

Linked Data

• gnomAD v3: 19-7212064-T-TCAGACTCTGGGGTGGATGATTCCCCCATCACTGTTATCTTAAAGTAGGGTTTCTCAGCCTCAGGAC
• gnomAD v4: 19-7212064-T-TCAGACTCTGGGGTGGATGATTCCCCCATCACTGTTATCTTAAAGTAGGGTTTCTCAGCCTCAGGAC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7212064_7212065insCAGACTCTGGGGTGGATGATTCCCCCATCACTGTTATCTTAAAGTAGGGTTTCTCAGCCTCAGGAC , CM000681.2:g.7212064_7212065insCAGACTCTGGGGTGGATGATTCCCCCATCACTGTTATCTTAAAGTAGGGTTTCTCAGCCTCAGGAC	GRCh38
NC_000019.9:g.7212075_7212076insCAGACTCTGGGGTGGATGATTCCCCCATCACTGTTATCTTAAAGTAGGGTTTCTCAGCCTCAGGAC , CM000681.1:g.7212075_7212076insCAGACTCTGGGGTGGATGATTCCCCCATCACTGTTATCTTAAAGTAGGGTTTCTCAGCCTCAGGAC	GRCh37
NC_000019.8:g.7163075_7163076insCAGACTCTGGGGTGGATGATTCCCCCATCACTGTTATCTTAAAGTAGGGTTTCTCAGCCTCAGGAC	NCBI36
NG_008852.2:g.86936_86937insGTCCTGAGGCTGAGAAACCCTACTTTAAGATAACAGTGATGGGGGAATCATCCACCCCAGAGTCTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-27428_653-27427insGTCCTGAGGCTGAGAAACCCTACTTTAAGATAACAGTGATGGGGGAATCATCCACCCCAGAGTCTG MANE Select	ENSP00000303830.4:n.653-27428_653-27427insGTCCTGAGGCTGAGAAACC...
ENST00000302850.9:c.653-27428_653-27427insGTCCTGAGGCTGAGAAACCCTACTTTAAGATAACAGTGATGGGGGAATCATCCACCCCAGAGTCTG	ENSP00000303830.4:n.653-27428_653-27427insGTCCTGAGGCTGAGAAACC...
ENST00000341500.9:c.653-27428_653-27427insGTCCTGAGGCTGAGAAACCCTACTTTAAGATAACAGTGATGGGGGAATCATCCACCCCAGAGTCTG	ENSP00000342838.4:n.653-27428_653-27427insGTCCTGAGGCTGAGAAACC...
ENST00000598216.1:n.628-27428_628-27427insGTCCTGAGGCTGAGAAACCCTACTTTAAGATAACAGTGATGGGGGAATCATCCACCCCAGAGTCTG
NM_000208.2:c.653-27428_653-27427insGTCCTGAGGCTGAGAAACCCTACTTTAAGATAACAGTGATGGGGGAATCATCCACCCCAGAGTCTG	NP_000199.2:n.653-27428_653-27427insGTCCTGAGGCTGAGAAACCCTACTT...
NM_000208.3:c.653-27428_653-27427insGTCCTGAGGCTGAGAAACCCTACTTTAAGATAACAGTGATGGGGGAATCATCCACCCCAGAGTCTG	NP_000199.2:n.653-27428_653-27427insGTCCTGAGGCTGAGAAACCCTACTT...
NM_001079817.1:c.653-27428_653-27427insGTCCTGAGGCTGAGAAACCCTACTTTAAGATAACAGTGATGGGGGAATCATCCACCCCAGAGTCTG	NP_001073285.1:n.653-27428_653-27427insGTCCTGAGGCTGAGAAACCCTA...
NM_001079817.2:c.653-27428_653-27427insGTCCTGAGGCTGAGAAACCCTACTTTAAGATAACAGTGATGGGGGAATCATCCACCCCAGAGTCTG	NP_001073285.1:n.653-27428_653-27427insGTCCTGAGGCTGAGAAACCCTA...
XM_011527988.1:c.731-27428_731-27427insGTCCTGAGGCTGAGAAACCCTACTTTAAGATAACAGTGATGGGGGAATCATCCACCCCAGAGTCTG	XP_011526290.1:n.731-27428_731-27427insGTCCTGAGGCTGAGAAACCCTA...
XM_011527989.1:c.731-27428_731-27427insGTCCTGAGGCTGAGAAACCCTACTTTAAGATAACAGTGATGGGGGAATCATCCACCCCAGAGTCTG	XP_011526291.1:n.731-27428_731-27427insGTCCTGAGGCTGAGAAACCCTA...
XM_011527988.2:c.653-27428_653-27427insGTCCTGAGGCTGAGAAACCCTACTTTAAGATAACAGTGATGGGGGAATCATCCACCCCAGAGTCTG	XP_011526290.2:n.653-27428_653-27427insGTCCTGAGGCTGAGAAACCCTA...
XM_011527989.3:c.653-27428_653-27427insGTCCTGAGGCTGAGAAACCCTACTTTAAGATAACAGTGATGGGGGAATCATCCACCCCAGAGTCTG	XP_011526291.2:n.653-27428_653-27427insGTCCTGAGGCTGAGAAACCCTA...
NM_000208.4:c.653-27428_653-27427insGTCCTGAGGCTGAGAAACCCTACTTTAAGATAACAGTGATGGGGGAATCATCCACCCCAGAGTCTG MANE Select	NP_000199.2:n.653-27428_653-27427insGTCCTGAGGCTGAGAAACCCTACTT...
NM_001079817.3:c.653-27428_653-27427insGTCCTGAGGCTGAGAAACCCTACTTTAAGATAACAGTGATGGGGGAATCATCCACCCCAGAGTCTG	NP_001073285.1:n.653-27428_653-27427insGTCCTGAGGCTGAGAAACCCTA...