Canonical Allele Identifier: CA2320763867

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117024_7117025delinsAC , CM000681.2:g.7117024_7117025delinsAC	GRCh38
NC_000019.9:g.7117035_7117036delinsAC , CM000681.1:g.7117035_7117036delinsAC	GRCh37
NC_000019.8:g.7068035_7068036delinsAC	NCBI36
NG_008852.2:g.181976_181977delinsGT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.*31_*32delinsGT MANE Select	ENSP00000303830.4:n.*31_*32delinsGT
ENST00000302850.9:c.*31_*32delinsGT	ENSP00000303830.4:n.*31_*32delinsGT
ENST00000341500.9:c.*31_*32delinsGT	ENSP00000342838.4:n.*31_*32delinsGT
NM_000208.2:c.*31_*32delinsGT	NP_000199.2:n.*31_*32delinsGT
NM_000208.3:c.*31_*32delinsGT	NP_000199.2:n.*31_*32delinsGT
NM_001079817.1:c.*31_*32delinsGT	NP_001073285.1:n.*31_*32delinsGT
NM_001079817.2:c.*31_*32delinsGT	NP_001073285.1:n.*31_*32delinsGT
XM_011527988.1:c.*31_*32delinsGT	XP_011526290.1:n.*31_*32delinsGT
XM_011527989.1:c.*31_*32delinsGT	XP_011526291.1:n.*31_*32delinsGT
XM_011527988.2:c.*31_*32delinsGT	XP_011526290.2:n.*31_*32delinsGT
XM_011527989.3:c.*31_*32delinsGT	XP_011526291.2:n.*31_*32delinsGT
NM_000208.4:c.*31_*32delinsGT MANE Select	NP_000199.2:n.*31_*32delinsGT
NM_001079817.3:c.*31_*32delinsGT	NP_001073285.1:n.*31_*32delinsGT