Canonical Allele Identifier: CA920049237
Gene: INSR HGNC NCBI

Linked Data

dbSNP Id: rs1599863076

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7116919del , CM000681.2:g.7116919del GRCh38
NC_000019.9:g.7116930del , CM000681.1:g.7116930del GRCh37
NC_000019.8:g.7067930del NCBI36
NG_008852.2:g.182083del

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.*138del MANE Select ENSP00000303830.4:n.*138del
ENST00000302850.9:c.*138del ENSP00000303830.4:n.*138del
ENST00000341500.9:c.*138del ENSP00000342838.4:n.*138del
NM_000208.2:c.*138del NP_000199.2:n.*138del
NM_000208.3:c.*138del NP_000199.2:n.*138del
NM_001079817.1:c.*138del NP_001073285.1:n.*138del
NM_001079817.2:c.*138del NP_001073285.1:n.*138del
XM_011527988.1:c.*138del XP_011526290.1:n.*138del
XM_011527989.1:c.*138del XP_011526291.1:n.*138del
XM_011527988.2:c.*138del XP_011526290.2:n.*138del
XM_011527989.3:c.*138del XP_011526291.2:n.*138del
NM_000208.4:c.*138del MANE Select NP_000199.2:n.*138del
NM_001079817.3:c.*138del NP_001073285.1:n.*138del