Canonical Allele Identifier: CA993122720

Gene: INSR

Linked Data

• gnomAD v3: 19-7212058-G-GCTGTTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTCCC
• gnomAD v4: 19-7212058-G-GCTGTTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTCCC

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7212059_7212060insTGTTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTCCCC , CM000681.2:g.7212059_7212060insTGTTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTCCCC	GRCh38
NC_000019.9:g.7212070_7212071insTGTTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTCCCC , CM000681.1:g.7212070_7212071insTGTTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTCCCC	GRCh37
NC_000019.8:g.7163070_7163071insTGTTTCCCAAGTCACAGACTCAGACTCTGGGGTGGATAATTCCCC	NCBI36
NG_008852.2:g.86942_86943insGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAACAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.653-27422_653-27421insGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAACAG MANE Select	ENSP00000303830.4:n.653-27422_653-27421insGGGAATTATCCACCCCAGA...
ENST00000302850.9:c.653-27422_653-27421insGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAACAG	ENSP00000303830.4:n.653-27422_653-27421insGGGAATTATCCACCCCAGA...
ENST00000341500.9:c.653-27422_653-27421insGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAACAG	ENSP00000342838.4:n.653-27422_653-27421insGGGAATTATCCACCCCAGA...
ENST00000598216.1:n.628-27422_628-27421insGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAACAG
NM_000208.2:c.653-27422_653-27421insGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAACAG	NP_000199.2:n.653-27422_653-27421insGGGAATTATCCACCCCAGAGTCTGA...
NM_000208.3:c.653-27422_653-27421insGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAACAG	NP_000199.2:n.653-27422_653-27421insGGGAATTATCCACCCCAGAGTCTGA...
NM_001079817.1:c.653-27422_653-27421insGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAACAG	NP_001073285.1:n.653-27422_653-27421insGGGAATTATCCACCCCAGAGTC...
NM_001079817.2:c.653-27422_653-27421insGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAACAG	NP_001073285.1:n.653-27422_653-27421insGGGAATTATCCACCCCAGAGTC...
XM_011527988.1:c.731-27422_731-27421insGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAACAG	XP_011526290.1:n.731-27422_731-27421insGGGAATTATCCACCCCAGAGTC...
XM_011527989.1:c.731-27422_731-27421insGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAACAG	XP_011526291.1:n.731-27422_731-27421insGGGAATTATCCACCCCAGAGTC...
XM_011527988.2:c.653-27422_653-27421insGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAACAG	XP_011526290.2:n.653-27422_653-27421insGGGAATTATCCACCCCAGAGTC...
XM_011527989.3:c.653-27422_653-27421insGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAACAG	XP_011526291.2:n.653-27422_653-27421insGGGAATTATCCACCCCAGAGTC...
NM_000208.4:c.653-27422_653-27421insGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAACAG MANE Select	NP_000199.2:n.653-27422_653-27421insGGGAATTATCCACCCCAGAGTCTGA...
NM_001079817.3:c.653-27422_653-27421insGGGAATTATCCACCCCAGAGTCTGAGTCTGTGACTTGGGAAACAG	NP_001073285.1:n.653-27422_653-27421insGGGAATTATCCACCCCAGAGTC...