Canonical Allele Identifier: CA2320809794
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7211712_7211713delinsAG , CM000681.2:g.7211712_7211713delinsAG GRCh38
NC_000019.9:g.7211723_7211724delinsAG , CM000681.1:g.7211723_7211724delinsAG GRCh37
NC_000019.8:g.7162723_7162724delinsAG NCBI36
NG_008852.2:g.87288_87289delinsCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.653-27076_653-27075delinsCT MANE Select ENSP00000303830.4:n.653-27076_653-27075delinsCT
ENST00000302850.9:c.653-27076_653-27075delinsCT ENSP00000303830.4:n.653-27076_653-27075delinsCT
ENST00000341500.9:c.653-27076_653-27075delinsCT ENSP00000342838.4:n.653-27076_653-27075delinsCT
ENST00000598216.1:n.628-27076_628-27075delinsCT
NM_000208.2:c.653-27076_653-27075delinsCT NP_000199.2:n.653-27076_653-27075delinsCT
NM_000208.3:c.653-27076_653-27075delinsCT NP_000199.2:n.653-27076_653-27075delinsCT
NM_001079817.1:c.653-27076_653-27075delinsCT NP_001073285.1:n.653-27076_653-27075delinsCT
NM_001079817.2:c.653-27076_653-27075delinsCT NP_001073285.1:n.653-27076_653-27075delinsCT
XM_011527988.1:c.731-27076_731-27075delinsCT XP_011526290.1:n.731-27076_731-27075delinsCT
XM_011527989.1:c.731-27076_731-27075delinsCT XP_011526291.1:n.731-27076_731-27075delinsCT
XM_011527988.2:c.653-27076_653-27075delinsCT XP_011526290.2:n.653-27076_653-27075delinsCT
XM_011527989.3:c.653-27076_653-27075delinsCT XP_011526291.2:n.653-27076_653-27075delinsCT
NM_000208.4:c.653-27076_653-27075delinsCT MANE Select NP_000199.2:n.653-27076_653-27075delinsCT
NM_001079817.3:c.653-27076_653-27075delinsCT NP_001073285.1:n.653-27076_653-27075delinsCT