Canonical Allele Identifier: CA2320769461

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128864_7128868delinsAATAG , CM000681.2:g.7128864_7128868delinsAATAG	GRCh38
NC_000019.9:g.7128875_7128879delinsAATAG , CM000681.1:g.7128875_7128879delinsAATAG	GRCh37
NC_000019.8:g.7079875_7079879delinsAATAG	NCBI36
NG_008852.2:g.170133_170137delinsCTATT

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2929_2933delinsCTATT MANE Select	ENSP00000303830.4:p.Leu977=
ENST00000302850.9:c.2929_2933delinsCTATT	ENSP00000303830.4:p.Leu977=
ENST00000341500.9:c.2893_2897delinsCTATT	ENSP00000342838.4:p.Leu965=
NM_000208.2:c.2929_2933delinsCTATT	NP_000199.2:p.Leu977=
NM_000208.3:c.2929_2933delinsCTATT	NP_000199.2:p.Leu977=
NM_001079817.1:c.2893_2897delinsCTATT	NP_001073285.1:p.Leu965=
NM_001079817.2:c.2893_2897delinsCTATT	NP_001073285.1:p.Leu965=
XM_011527988.1:c.3004_3008delinsCTATT	XP_011526290.1:p.Leu1002=
XM_011527989.1:c.2968_2972delinsCTATT	XP_011526291.1:p.Leu990=
XM_011527988.2:c.2926_2930delinsCTATT	XP_011526290.2:p.Leu976=
XM_011527989.3:c.2890_2894delinsCTATT	XP_011526291.2:p.Leu964=
NM_000208.4:c.2929_2933delinsCTATT MANE Select	NP_000199.2:p.Leu977=
NM_001079817.3:c.2893_2897delinsCTATT	NP_001073285.1:p.Leu965=