Canonical Allele Identifier: CA993122774

Gene: INSR

Linked Data

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

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7212064_7212065insCAGACTCTGGGGTGGATAATTCCCCCATCAC , CM000681.2:g.7212064_7212065insCAGACTCTGGGGTGGATAATTCCCCCATCAC	GRCh38
NC_000019.9:g.7212075_7212076insCAGACTCTGGGGTGGATAATTCCCCCATCAC , CM000681.1:g.7212075_7212076insCAGACTCTGGGGTGGATAATTCCCCCATCAC	GRCh37
NC_000019.8:g.7163075_7163076insCAGACTCTGGGGTGGATAATTCCCCCATCAC	NCBI36
NG_008852.2:g.86936_86937insGTGATGGGGGAATTATCCACCCCAGAGTCTG

Transcript Alleles

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