Canonical Allele Identifier: CA2320763643

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116766_7116767delinsGT , CM000681.2:g.7116766_7116767delinsGT	GRCh38
NC_000019.9:g.7116777_7116778delinsGT , CM000681.1:g.7116777_7116778delinsGT	GRCh37
NC_000019.8:g.7067777_7067778delinsGT	NCBI36
NG_008852.2:g.182234_182235delinsAC

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.*289_*290delinsAC MANE Select	ENSP00000303830.4:n.*289_*290delinsAC
ENST00000302850.9:c.*289_*290delinsAC	ENSP00000303830.4:n.*289_*290delinsAC
ENST00000341500.9:c.*289_*290delinsAC	ENSP00000342838.4:n.*289_*290delinsAC
NM_000208.2:c.*289_*290delinsAC	NP_000199.2:n.*289_*290delinsAC
NM_000208.3:c.*289_*290delinsAC	NP_000199.2:n.*289_*290delinsAC
NM_001079817.1:c.*289_*290delinsAC	NP_001073285.1:n.*289_*290delinsAC
NM_001079817.2:c.*289_*290delinsAC	NP_001073285.1:n.*289_*290delinsAC
XM_011527988.1:c.*289_*290delinsAC	XP_011526290.1:n.*289_*290delinsAC
XM_011527989.1:c.*289_*290delinsAC	XP_011526291.1:n.*289_*290delinsAC
XM_011527988.2:c.*289_*290delinsAC	XP_011526290.2:n.*289_*290delinsAC
XM_011527989.3:c.*289_*290delinsAC	XP_011526291.2:n.*289_*290delinsAC
NM_000208.4:c.*289_*290delinsAC MANE Select	NP_000199.2:n.*289_*290delinsAC
NM_001079817.3:c.*289_*290delinsAC	NP_001073285.1:n.*289_*290delinsAC