Canonical Allele Identifier: CA2320763638
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7116762_7116763delinsGC , CM000681.2:g.7116762_7116763delinsGC GRCh38
NC_000019.9:g.7116773_7116774delinsGC , CM000681.1:g.7116773_7116774delinsGC GRCh37
NC_000019.8:g.7067773_7067774delinsGC NCBI36
NG_008852.2:g.182238_182239delinsGC

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.*293_*294delinsGC MANE Select ENSP00000303830.4:n.*293_*294delinsGC
ENST00000302850.9:c.*293_*294delinsGC ENSP00000303830.4:n.*293_*294delinsGC
ENST00000341500.9:c.*293_*294delinsGC ENSP00000342838.4:n.*293_*294delinsGC
NM_000208.2:c.*293_*294delinsGC NP_000199.2:n.*293_*294delinsGC
NM_000208.3:c.*293_*294delinsGC NP_000199.2:n.*293_*294delinsGC
NM_001079817.1:c.*293_*294delinsGC NP_001073285.1:n.*293_*294delinsGC
NM_001079817.2:c.*293_*294delinsGC NP_001073285.1:n.*293_*294delinsGC
XM_011527988.1:c.*293_*294delinsGC XP_011526290.1:n.*293_*294delinsGC
XM_011527989.1:c.*293_*294delinsGC XP_011526291.1:n.*293_*294delinsGC
XM_011527988.2:c.*293_*294delinsGC XP_011526290.2:n.*293_*294delinsGC
XM_011527989.3:c.*293_*294delinsGC XP_011526291.2:n.*293_*294delinsGC
NM_000208.4:c.*293_*294delinsGC MANE Select NP_000199.2:n.*293_*294delinsGC
NM_001079817.3:c.*293_*294delinsGC NP_001073285.1:n.*293_*294delinsGC