Canonical Allele Identifier: CA9135066
Gene: INSR HGNC NCBI

Linked Data

dbSNP Id: rs777967988

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7117028del , CM000681.2:g.7117028del GRCh38
NC_000019.9:g.7117039del , CM000681.1:g.7117039del GRCh37
NC_000019.8:g.7068039del NCBI36
NG_008852.2:g.181976del

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.*31del MANE Select ENSP00000303830.4:n.*31del
ENST00000302850.9:c.*31del ENSP00000303830.4:n.*31del
ENST00000341500.9:c.*31del ENSP00000342838.4:n.*31del
NM_000208.2:c.*31del NP_000199.2:n.*31del
NM_000208.3:c.*31del NP_000199.2:n.*31del
NM_001079817.1:c.*31del NP_001073285.1:n.*31del
NM_001079817.2:c.*31del NP_001073285.1:n.*31del
XM_011527988.1:c.*31del XP_011526290.1:n.*31del
XM_011527989.1:c.*31del XP_011526291.1:n.*31del
XM_011527988.2:c.*31del XP_011526290.2:n.*31del
XM_011527989.3:c.*31del XP_011526291.2:n.*31del
NM_000208.4:c.*31del MANE Select NP_000199.2:n.*31del
NM_001079817.3:c.*31del NP_001073285.1:n.*31del