Canonical Allele Identifier: CA2521661802

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166688_7166689insGTGGGC , CM000681.2:g.7166688_7166689insGTGGGC	GRCh38
NC_000019.9:g.7166699_7166700insGTGGGC , CM000681.1:g.7166699_7166700insGTGGGC	GRCh37
NC_000019.8:g.7117699_7117700insGTGGGC	NCBI36
NG_008852.2:g.132312_132313insGCCCAC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.1611-285_1611-284insGCCCAC MANE Select	ENSP00000303830.4:n.1611-285_1611-284insGCCCAC
ENST00000302850.9:c.1611-285_1611-284insGCCCAC	ENSP00000303830.4:n.1611-285_1611-284insGCCCAC
ENST00000341500.9:c.1611-285_1611-284insGCCCAC	ENSP00000342838.4:n.1611-285_1611-284insGCCCAC
ENST00000598216.1:n.1586-285_1586-284insGCCCAC
ENST00000600492.1:c.12-285_12-284insGCCCAC	ENSP00000473170.1:n.12-285_12-284insGCCCAC
NM_000208.2:c.1611-285_1611-284insGCCCAC	NP_000199.2:n.1611-285_1611-284insGCCCAC
NM_000208.3:c.1611-285_1611-284insGCCCAC	NP_000199.2:n.1611-285_1611-284insGCCCAC
NM_001079817.1:c.1611-285_1611-284insGCCCAC	NP_001073285.1:n.1611-285_1611-284insGCCCAC
NM_001079817.2:c.1611-285_1611-284insGCCCAC	NP_001073285.1:n.1611-285_1611-284insGCCCAC
XM_011527988.1:c.1689-285_1689-284insGCCCAC	XP_011526290.1:n.1689-285_1689-284insGCCCAC
XM_011527989.1:c.1689-285_1689-284insGCCCAC	XP_011526291.1:n.1689-285_1689-284insGCCCAC
XM_011527988.2:c.1611-285_1611-284insGCCCAC	XP_011526290.2:n.1611-285_1611-284insGCCCAC
XM_011527989.3:c.1611-285_1611-284insGCCCAC	XP_011526291.2:n.1611-285_1611-284insGCCCAC
NM_000208.4:c.1611-285_1611-284insGCCCAC MANE Select	NP_000199.2:n.1611-285_1611-284insGCCCAC
NM_001079817.3:c.1611-285_1611-284insGCCCAC	NP_001073285.1:n.1611-285_1611-284insGCCCAC