Canonical Allele Identifier: CA2813449667

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116773_7116774insGGGGT , CM000681.2:g.7116773_7116774insGGGGT	GRCh38
NC_000019.9:g.7116784_7116785insGGGGT , CM000681.1:g.7116784_7116785insGGGGT	GRCh37
NC_000019.8:g.7067784_7067785insGGGGT	NCBI36
NG_008852.2:g.182227_182228insACCCC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.*282_*283insACCCC MANE Select	ENSP00000303830.4:n.*282_*283insACCCC
ENST00000302850.9:c.*282_*283insACCCC	ENSP00000303830.4:n.*282_*283insACCCC
ENST00000341500.9:c.*282_*283insACCCC	ENSP00000342838.4:n.*282_*283insACCCC
NM_000208.2:c.*282_*283insACCCC	NP_000199.2:n.*282_*283insACCCC
NM_000208.3:c.*282_*283insACCCC	NP_000199.2:n.*282_*283insACCCC
NM_001079817.1:c.*282_*283insACCCC	NP_001073285.1:n.*282_*283insACCCC
NM_001079817.2:c.*282_*283insACCCC	NP_001073285.1:n.*282_*283insACCCC
XM_011527988.1:c.*282_*283insACCCC	XP_011526290.1:n.*282_*283insACCCC
XM_011527989.1:c.*282_*283insACCCC	XP_011526291.1:n.*282_*283insACCCC
XM_011527988.2:c.*282_*283insACCCC	XP_011526290.2:n.*282_*283insACCCC
XM_011527989.3:c.*282_*283insACCCC	XP_011526291.2:n.*282_*283insACCCC
NM_000208.4:c.*282_*283insACCCC MANE Select	NP_000199.2:n.*282_*283insACCCC
NM_001079817.3:c.*282_*283insACCCC	NP_001073285.1:n.*282_*283insACCCC