Canonical Allele Identifier: CA2582314749
Gene: INSR HGNC NCBI

Linked Data

dbSNP Id: rs2144990763

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7184705_7184706insGTAAATAA , CM000681.2:g.7184705_7184706insGTAAATAA GRCh38
NC_000019.9:g.7184716_7184717insGTAAATAA , CM000681.1:g.7184716_7184717insGTAAATAA GRCh37
NC_000019.8:g.7135716_7135717insGTAAATAA NCBI36
NG_008852.2:g.114302_114303insCTTATTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.653-62_653-61insCTTATTTA MANE Select ENSP00000303830.4:n.653-62_653-61insCTTATTTA
ENST00000302850.9:c.653-62_653-61insCTTATTTA ENSP00000303830.4:n.653-62_653-61insCTTATTTA
ENST00000341500.9:c.653-62_653-61insCTTATTTA ENSP00000342838.4:n.653-62_653-61insCTTATTTA
ENST00000598216.1:n.628-62_628-61insCTTATTTA
NM_000208.2:c.653-62_653-61insCTTATTTA NP_000199.2:n.653-62_653-61insCTTATTTA
NM_000208.3:c.653-62_653-61insCTTATTTA NP_000199.2:n.653-62_653-61insCTTATTTA
NM_001079817.1:c.653-62_653-61insCTTATTTA NP_001073285.1:n.653-62_653-61insCTTATTTA
NM_001079817.2:c.653-62_653-61insCTTATTTA NP_001073285.1:n.653-62_653-61insCTTATTTA
XM_011527988.1:c.731-62_731-61insCTTATTTA XP_011526290.1:n.731-62_731-61insCTTATTTA
XM_011527989.1:c.731-62_731-61insCTTATTTA XP_011526291.1:n.731-62_731-61insCTTATTTA
XM_011527988.2:c.653-62_653-61insCTTATTTA XP_011526290.2:n.653-62_653-61insCTTATTTA
XM_011527989.3:c.653-62_653-61insCTTATTTA XP_011526291.2:n.653-62_653-61insCTTATTTA
NM_000208.4:c.653-62_653-61insCTTATTTA MANE Select NP_000199.2:n.653-62_653-61insCTTATTTA
NM_001079817.3:c.653-62_653-61insCTTATTTA NP_001073285.1:n.653-62_653-61insCTTATTTA