Canonical Allele Identifier: CA920049762
Gene: INSR HGNC NCBI

Linked Data

dbSNP Id: rs1555753061

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7211717_7211718delinsT , CM000681.2:g.7211717_7211718delinsT GRCh38
NC_000019.9:g.7211728_7211729delinsT , CM000681.1:g.7211728_7211729delinsT GRCh37
NC_000019.8:g.7162728_7162729delinsT NCBI36
NG_008852.2:g.87283_87284delinsA

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.653-27081_653-27080delinsA MANE Select ENSP00000303830.4:n.653-27081_653-27080delinsA
ENST00000302850.9:c.653-27081_653-27080delinsA ENSP00000303830.4:n.653-27081_653-27080delinsA
ENST00000341500.9:c.653-27081_653-27080delinsA ENSP00000342838.4:n.653-27081_653-27080delinsA
ENST00000598216.1:n.628-27081_628-27080delinsA
NM_000208.2:c.653-27081_653-27080delinsA NP_000199.2:n.653-27081_653-27080delinsA
NM_000208.3:c.653-27081_653-27080delinsA NP_000199.2:n.653-27081_653-27080delinsA
NM_001079817.1:c.653-27081_653-27080delinsA NP_001073285.1:n.653-27081_653-27080delinsA
NM_001079817.2:c.653-27081_653-27080delinsA NP_001073285.1:n.653-27081_653-27080delinsA
XM_011527988.1:c.731-27081_731-27080delinsA XP_011526290.1:n.731-27081_731-27080delinsA
XM_011527989.1:c.731-27081_731-27080delinsA XP_011526291.1:n.731-27081_731-27080delinsA
XM_011527988.2:c.653-27081_653-27080delinsA XP_011526290.2:n.653-27081_653-27080delinsA
XM_011527989.3:c.653-27081_653-27080delinsA XP_011526291.2:n.653-27081_653-27080delinsA
NM_000208.4:c.653-27081_653-27080delinsA MANE Select NP_000199.2:n.653-27081_653-27080delinsA
NM_001079817.3:c.653-27081_653-27080delinsA NP_001073285.1:n.653-27081_653-27080delinsA