Canonical Allele Identifier: CA2320779442

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7150370_7150382delinsCTCTCCAGCACAG , CM000681.2:g.7150370_7150382delinsCTCTCCAGCACAG	GRCh38
NC_000019.9:g.7150381_7150393delinsCTCTCCAGCACAG , CM000681.1:g.7150381_7150393delinsCTCTCCAGCACAG	GRCh37
NC_000019.8:g.7101381_7101393delinsCTCTCCAGCACAG	NCBI36
NG_008852.2:g.148619_148631delinsCTGTGCTGGAGAG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2267+115_2267+127delinsCTGTGCTGGAGAG MANE Select	ENSP00000303830.4:n.2267+115_2267+127delinsCTGTGCTGGAGAG
ENST00000302850.9:c.2267+115_2267+127delinsCTGTGCTGGAGAG	ENSP00000303830.4:n.2267+115_2267+127delinsCTGTGCTGGAGAG
ENST00000341500.9:c.2231+2344_2231+2356delinsCTGTGCTGGAGAG	ENSP00000342838.4:n.2231+2344_2231+2356delinsCTGTGCTGGAGAG
NM_000208.2:c.2267+115_2267+127delinsCTGTGCTGGAGAG	NP_000199.2:n.2267+115_2267+127delinsCTGTGCTGGAGAG
NM_000208.3:c.2267+115_2267+127delinsCTGTGCTGGAGAG	NP_000199.2:n.2267+115_2267+127delinsCTGTGCTGGAGAG
NM_001079817.1:c.2231+2344_2231+2356delinsCTGTGCTGGAGAG	NP_001073285.1:n.2231+2344_2231+2356delinsCTGTGCTGGAGAG
NM_001079817.2:c.2231+2344_2231+2356delinsCTGTGCTGGAGAG	NP_001073285.1:n.2231+2344_2231+2356delinsCTGTGCTGGAGAG
XM_011527988.1:c.2345+115_2345+127delinsCTGTGCTGGAGAG	XP_011526290.1:n.2345+115_2345+127delinsCTGTGCTGGAGAG
XM_011527989.1:c.2309+2344_2309+2356delinsCTGTGCTGGAGAG	XP_011526291.1:n.2309+2344_2309+2356delinsCTGTGCTGGAGAG
XM_011527988.2:c.2267+115_2267+127delinsCTGTGCTGGAGAG	XP_011526290.2:n.2267+115_2267+127delinsCTGTGCTGGAGAG
XM_011527989.3:c.2231+2344_2231+2356delinsCTGTGCTGGAGAG	XP_011526291.2:n.2231+2344_2231+2356delinsCTGTGCTGGAGAG
NM_000208.4:c.2267+115_2267+127delinsCTGTGCTGGAGAG MANE Select	NP_000199.2:n.2267+115_2267+127delinsCTGTGCTGGAGAG
NM_001079817.3:c.2231+2344_2231+2356delinsCTGTGCTGGAGAG	NP_001073285.1:n.2231+2344_2231+2356delinsCTGTGCTGGAGAG