Canonical Allele Identifier: CA2587926418

Gene: INSR

Linked Data

• gnomAD v4: 19-7184680-A-AAATC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7184683_7184684insCAAT , CM000681.2:g.7184683_7184684insCAAT	GRCh38
NC_000019.9:g.7184694_7184695insCAAT , CM000681.1:g.7184694_7184695insCAAT	GRCh37
NC_000019.8:g.7135694_7135695insCAAT	NCBI36
NG_008852.2:g.114320_114321insGATT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-44_653-43insGATT MANE Select	ENSP00000303830.4:n.653-44_653-43insGATT
ENST00000302850.9:c.653-44_653-43insGATT	ENSP00000303830.4:n.653-44_653-43insGATT
ENST00000341500.9:c.653-44_653-43insGATT	ENSP00000342838.4:n.653-44_653-43insGATT
ENST00000598216.1:n.628-44_628-43insGATT
NM_000208.2:c.653-44_653-43insGATT	NP_000199.2:n.653-44_653-43insGATT
NM_000208.3:c.653-44_653-43insGATT	NP_000199.2:n.653-44_653-43insGATT
NM_001079817.1:c.653-44_653-43insGATT	NP_001073285.1:n.653-44_653-43insGATT
NM_001079817.2:c.653-44_653-43insGATT	NP_001073285.1:n.653-44_653-43insGATT
XM_011527988.1:c.731-44_731-43insGATT	XP_011526290.1:n.731-44_731-43insGATT
XM_011527989.1:c.731-44_731-43insGATT	XP_011526291.1:n.731-44_731-43insGATT
XM_011527988.2:c.653-44_653-43insGATT	XP_011526290.2:n.653-44_653-43insGATT
XM_011527989.3:c.653-44_653-43insGATT	XP_011526291.2:n.653-44_653-43insGATT
NM_000208.4:c.653-44_653-43insGATT MANE Select	NP_000199.2:n.653-44_653-43insGATT
NM_001079817.3:c.653-44_653-43insGATT	NP_001073285.1:n.653-44_653-43insGATT