Canonical Allele Identifier: CA2320763671
Gene: INSR HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000019.10:g.7116805_7116806delinsCG , CM000681.2:g.7116805_7116806delinsCG GRCh38
NC_000019.9:g.7116816_7116817delinsCG , CM000681.1:g.7116816_7116817delinsCG GRCh37
NC_000019.8:g.7067816_7067817delinsCG NCBI36
NG_008852.2:g.182195_182196delinsCG

Transcript Alleles

HGVS Amino-acid change
ENST00000302850.10:c.*250_*251delinsCG MANE Select ENSP00000303830.4:n.*250_*251delinsCG
ENST00000302850.9:c.*250_*251delinsCG ENSP00000303830.4:n.*250_*251delinsCG
ENST00000341500.9:c.*250_*251delinsCG ENSP00000342838.4:n.*250_*251delinsCG
NM_000208.2:c.*250_*251delinsCG NP_000199.2:n.*250_*251delinsCG
NM_000208.3:c.*250_*251delinsCG NP_000199.2:n.*250_*251delinsCG
NM_001079817.1:c.*250_*251delinsCG NP_001073285.1:n.*250_*251delinsCG
NM_001079817.2:c.*250_*251delinsCG NP_001073285.1:n.*250_*251delinsCG
XM_011527988.1:c.*250_*251delinsCG XP_011526290.1:n.*250_*251delinsCG
XM_011527989.1:c.*250_*251delinsCG XP_011526291.1:n.*250_*251delinsCG
XM_011527988.2:c.*250_*251delinsCG XP_011526290.2:n.*250_*251delinsCG
XM_011527989.3:c.*250_*251delinsCG XP_011526291.2:n.*250_*251delinsCG
NM_000208.4:c.*250_*251delinsCG MANE Select NP_000199.2:n.*250_*251delinsCG
NM_001079817.3:c.*250_*251delinsCG NP_001073285.1:n.*250_*251delinsCG