Canonical Allele Identifier: CA9136054
Gene: INSR HGNC NCBI

Linked Data

dbSNP Id: rs199750451

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7184661_7184662insAGAGAGAGAGAGAGA , CM000681.2:g.7184661_7184662insAGAGAGAGAGAGAGA GRCh38
NC_000019.9:g.7184672_7184673insAGAGAGAGAGAGAGA , CM000681.1:g.7184672_7184673insAGAGAGAGAGAGAGA GRCh37
NC_000019.8:g.7135672_7135673insAGAGAGAGAGAGAGA NCBI36
NG_008852.2:g.114339_114340insTCTCTCTCTCTCTCT

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.653-25_653-24insTCTCTCTCTCTCTCT MANE Select ENSP00000303830.4:n.653-25_653-24insTCTCTCTCTCTCTCT
ENST00000302850.9:c.653-25_653-24insTCTCTCTCTCTCTCT ENSP00000303830.4:n.653-25_653-24insTCTCTCTCTCTCTCT
ENST00000341500.9:c.653-25_653-24insTCTCTCTCTCTCTCT ENSP00000342838.4:n.653-25_653-24insTCTCTCTCTCTCTCT
ENST00000598216.1:n.628-25_628-24insTCTCTCTCTCTCTCT
NM_000208.2:c.653-25_653-24insTCTCTCTCTCTCTCT NP_000199.2:n.653-25_653-24insTCTCTCTCTCTCTCT
NM_000208.3:c.653-25_653-24insTCTCTCTCTCTCTCT NP_000199.2:n.653-25_653-24insTCTCTCTCTCTCTCT
NM_001079817.1:c.653-25_653-24insTCTCTCTCTCTCTCT NP_001073285.1:n.653-25_653-24insTCTCTCTCTCTCTCT
NM_001079817.2:c.653-25_653-24insTCTCTCTCTCTCTCT NP_001073285.1:n.653-25_653-24insTCTCTCTCTCTCTCT
XM_011527988.1:c.731-25_731-24insTCTCTCTCTCTCTCT XP_011526290.1:n.731-25_731-24insTCTCTCTCTCTCTCT
XM_011527989.1:c.731-25_731-24insTCTCTCTCTCTCTCT XP_011526291.1:n.731-25_731-24insTCTCTCTCTCTCTCT
XM_011527988.2:c.653-25_653-24insTCTCTCTCTCTCTCT XP_011526290.2:n.653-25_653-24insTCTCTCTCTCTCTCT
XM_011527989.3:c.653-25_653-24insTCTCTCTCTCTCTCT XP_011526291.2:n.653-25_653-24insTCTCTCTCTCTCTCT
NM_000208.4:c.653-25_653-24insTCTCTCTCTCTCTCT MANE Select NP_000199.2:n.653-25_653-24insTCTCTCTCTCTCTCT
NM_001079817.3:c.653-25_653-24insTCTCTCTCTCTCTCT NP_001073285.1:n.653-25_653-24insTCTCTCTCTCTCTCT