Canonical Allele Identifier: CA2587926423
Gene: INSR HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7184685_7184686insCTAA , CM000681.2:g.7184685_7184686insCTAA GRCh38
NC_000019.9:g.7184696_7184697insCTAA , CM000681.1:g.7184696_7184697insCTAA GRCh37
NC_000019.8:g.7135696_7135697insCTAA NCBI36
NG_008852.2:g.114318_114319insGTTA

Transcript Alleles

HGVS Amino-acid Change
ENST00000302850.10:c.653-46_653-45insGTTA MANE Select ENSP00000303830.4:n.653-46_653-45insGTTA
ENST00000302850.9:c.653-46_653-45insGTTA ENSP00000303830.4:n.653-46_653-45insGTTA
ENST00000341500.9:c.653-46_653-45insGTTA ENSP00000342838.4:n.653-46_653-45insGTTA
ENST00000598216.1:n.628-46_628-45insGTTA
NM_000208.2:c.653-46_653-45insGTTA NP_000199.2:n.653-46_653-45insGTTA
NM_000208.3:c.653-46_653-45insGTTA NP_000199.2:n.653-46_653-45insGTTA
NM_001079817.1:c.653-46_653-45insGTTA NP_001073285.1:n.653-46_653-45insGTTA
NM_001079817.2:c.653-46_653-45insGTTA NP_001073285.1:n.653-46_653-45insGTTA
XM_011527988.1:c.731-46_731-45insGTTA XP_011526290.1:n.731-46_731-45insGTTA
XM_011527989.1:c.731-46_731-45insGTTA XP_011526291.1:n.731-46_731-45insGTTA
XM_011527988.2:c.653-46_653-45insGTTA XP_011526290.2:n.653-46_653-45insGTTA
XM_011527989.3:c.653-46_653-45insGTTA XP_011526291.2:n.653-46_653-45insGTTA
NM_000208.4:c.653-46_653-45insGTTA MANE Select NP_000199.2:n.653-46_653-45insGTTA
NM_001079817.3:c.653-46_653-45insGTTA NP_001073285.1:n.653-46_653-45insGTTA