Canonical Allele Identifier: CA2320763802
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7116925_7116926delinsAT , CM000681.2:g.7116925_7116926delinsAT GRCh38
NC_000019.9:g.7116936_7116937delinsAT , CM000681.1:g.7116936_7116937delinsAT GRCh37
NC_000019.8:g.7067936_7067937delinsAT NCBI36
NG_008852.2:g.182075_182076delinsAT

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.*130_*131delinsAT MANE Select ENSP00000303830.4:n.*130_*131delinsAT
ENST00000302850.9:c.*130_*131delinsAT ENSP00000303830.4:n.*130_*131delinsAT
ENST00000341500.9:c.*130_*131delinsAT ENSP00000342838.4:n.*130_*131delinsAT
NM_000208.2:c.*130_*131delinsAT NP_000199.2:n.*130_*131delinsAT
NM_000208.3:c.*130_*131delinsAT NP_000199.2:n.*130_*131delinsAT
NM_001079817.1:c.*130_*131delinsAT NP_001073285.1:n.*130_*131delinsAT
NM_001079817.2:c.*130_*131delinsAT NP_001073285.1:n.*130_*131delinsAT
XM_011527988.1:c.*130_*131delinsAT XP_011526290.1:n.*130_*131delinsAT
XM_011527989.1:c.*130_*131delinsAT XP_011526291.1:n.*130_*131delinsAT
XM_011527988.2:c.*130_*131delinsAT XP_011526290.2:n.*130_*131delinsAT
XM_011527989.3:c.*130_*131delinsAT XP_011526291.2:n.*130_*131delinsAT
NM_000208.4:c.*130_*131delinsAT MANE Select NP_000199.2:n.*130_*131delinsAT
NM_001079817.3:c.*130_*131delinsAT NP_001073285.1:n.*130_*131delinsAT