Canonical Allele Identifier: CA645607106

Gene: INSR

Linked Data

• COSMIC: COSM5833898 ; COSM5833899
• PubMed: PMID:27479843

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7152738del , CM000681.2:g.7152738del	GRCh38
NC_000019.9:g.7152749del , CM000681.1:g.7152749del	GRCh37
NC_000019.8:g.7103749del	NCBI36
NG_008852.2:g.146266del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2222del MANE Select	ENSP00000303830.4:p.Phe741SerfsTer30
ENST00000302850.9:c.2222del	ENSP00000303830.4:p.Phe741SerfsTer30
ENST00000341500.9:c.2222del	ENSP00000342838.4:p.Phe741SerfsTer18
ENST00000598216.1:n.2197del
NM_000208.2:c.2222del	NP_000199.2:p.Phe741SerfsTer30
NM_000208.3:c.2222del	NP_000199.2:p.Phe741SerfsTer30
NM_001079817.1:c.2222del	NP_001073285.1:p.Phe741SerfsTer18
NM_001079817.2:c.2222del	NP_001073285.1:p.Phe741SerfsTer18
XM_011527988.1:c.2300del	XP_011526290.1:p.Phe767SerfsTer30
XM_011527989.1:c.2300del	XP_011526291.1:p.Phe767SerfsTer18
XM_011527988.2:c.2222del	XP_011526290.2:p.Phe741SerfsTer30
XM_011527989.3:c.2222del	XP_011526291.2:p.Phe741SerfsTer18
NM_000208.4:c.2222del MANE Select	NP_000199.2:p.Phe741SerfsTer30
NM_001079817.3:c.2222del	NP_001073285.1:p.Phe741SerfsTer18