Canonical Allele Identifier: CA2497029358

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7116767_7116768delinsTG , CM000681.2:g.7116767_7116768delinsTG	GRCh38
NC_000019.9:g.7116778_7116779delinsTG , CM000681.1:g.7116778_7116779delinsTG	GRCh37
NC_000019.8:g.7067778_7067779delinsTG	NCBI36
NG_008852.2:g.182233_182234delinsCA

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.*288_*289delinsCA MANE Select	ENSP00000303830.4:n.*288_*289delinsCA
ENST00000302850.9:c.*288_*289delinsCA	ENSP00000303830.4:n.*288_*289delinsCA
ENST00000341500.9:c.*288_*289delinsCA	ENSP00000342838.4:n.*288_*289delinsCA
NM_000208.2:c.*288_*289delinsCA	NP_000199.2:n.*288_*289delinsCA
NM_000208.3:c.*288_*289delinsCA	NP_000199.2:n.*288_*289delinsCA
NM_001079817.1:c.*288_*289delinsCA	NP_001073285.1:n.*288_*289delinsCA
NM_001079817.2:c.*288_*289delinsCA	NP_001073285.1:n.*288_*289delinsCA
XM_011527988.1:c.*288_*289delinsCA	XP_011526290.1:n.*288_*289delinsCA
XM_011527989.1:c.*288_*289delinsCA	XP_011526291.1:n.*288_*289delinsCA
XM_011527988.2:c.*288_*289delinsCA	XP_011526290.2:n.*288_*289delinsCA
XM_011527989.3:c.*288_*289delinsCA	XP_011526291.2:n.*288_*289delinsCA
NM_000208.4:c.*288_*289delinsCA MANE Select	NP_000199.2:n.*288_*289delinsCA
NM_001079817.3:c.*288_*289delinsCA	NP_001073285.1:n.*288_*289delinsCA