Canonical Allele Identifier: CA2320763831

Gene: INSR

Linked Data

• dbSNP Id: rs1972343818

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116963_7116964insCC , CM000681.2:g.7116963_7116964insCC	GRCh38
NC_000019.9:g.7116974_7116975insCC , CM000681.1:g.7116974_7116975insCC	GRCh37
NC_000019.8:g.7067974_7067975insCC	NCBI36
NG_008852.2:g.182037_182038insGG

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.*92_*93insGG MANE Select	ENSP00000303830.4:n.*92_*93insGG
ENST00000302850.9:c.*92_*93insGG	ENSP00000303830.4:n.*92_*93insGG
ENST00000341500.9:c.*92_*93insGG	ENSP00000342838.4:n.*92_*93insGG
NM_000208.2:c.*92_*93insGG	NP_000199.2:n.*92_*93insGG
NM_000208.3:c.*92_*93insGG	NP_000199.2:n.*92_*93insGG
NM_001079817.1:c.*92_*93insGG	NP_001073285.1:n.*92_*93insGG
NM_001079817.2:c.*92_*93insGG	NP_001073285.1:n.*92_*93insGG
XM_011527988.1:c.*92_*93insGG	XP_011526290.1:n.*92_*93insGG
XM_011527989.1:c.*92_*93insGG	XP_011526291.1:n.*92_*93insGG
XM_011527988.2:c.*92_*93insGG	XP_011526290.2:n.*92_*93insGG
XM_011527989.3:c.*92_*93insGG	XP_011526291.2:n.*92_*93insGG
NM_000208.4:c.*92_*93insGG MANE Select	NP_000199.2:n.*92_*93insGG
NM_001079817.3:c.*92_*93insGG	NP_001073285.1:n.*92_*93insGG