Canonical Allele Identifier: CA2320779443

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7150376_7150383delinsAGCACAGC , CM000681.2:g.7150376_7150383delinsAGCACAGC	GRCh38
NC_000019.9:g.7150387_7150394delinsAGCACAGC , CM000681.1:g.7150387_7150394delinsAGCACAGC	GRCh37
NC_000019.8:g.7101387_7101394delinsAGCACAGC	NCBI36
NG_008852.2:g.148618_148625delinsGCTGTGCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2267+114_2267+121delinsGCTGTGCT MANE Select	ENSP00000303830.4:n.2267+114_2267+121delinsGCTGTGCT
ENST00000302850.9:c.2267+114_2267+121delinsGCTGTGCT	ENSP00000303830.4:n.2267+114_2267+121delinsGCTGTGCT
ENST00000341500.9:c.2231+2343_2231+2350delinsGCTGTGCT	ENSP00000342838.4:n.2231+2343_2231+2350delinsGCTGTGCT
NM_000208.2:c.2267+114_2267+121delinsGCTGTGCT	NP_000199.2:n.2267+114_2267+121delinsGCTGTGCT
NM_000208.3:c.2267+114_2267+121delinsGCTGTGCT	NP_000199.2:n.2267+114_2267+121delinsGCTGTGCT
NM_001079817.1:c.2231+2343_2231+2350delinsGCTGTGCT	NP_001073285.1:n.2231+2343_2231+2350delinsGCTGTGCT
NM_001079817.2:c.2231+2343_2231+2350delinsGCTGTGCT	NP_001073285.1:n.2231+2343_2231+2350delinsGCTGTGCT
XM_011527988.1:c.2345+114_2345+121delinsGCTGTGCT	XP_011526290.1:n.2345+114_2345+121delinsGCTGTGCT
XM_011527989.1:c.2309+2343_2309+2350delinsGCTGTGCT	XP_011526291.1:n.2309+2343_2309+2350delinsGCTGTGCT
XM_011527988.2:c.2267+114_2267+121delinsGCTGTGCT	XP_011526290.2:n.2267+114_2267+121delinsGCTGTGCT
XM_011527989.3:c.2231+2343_2231+2350delinsGCTGTGCT	XP_011526291.2:n.2231+2343_2231+2350delinsGCTGTGCT
NM_000208.4:c.2267+114_2267+121delinsGCTGTGCT MANE Select	NP_000199.2:n.2267+114_2267+121delinsGCTGTGCT
NM_001079817.3:c.2231+2343_2231+2350delinsGCTGTGCT	NP_001073285.1:n.2231+2343_2231+2350delinsGCTGTGCT