Canonical Allele Identifier: CA2320776253

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7142990T= , CM000681.2:g.7142990T=	GRCh38
NC_000019.9:g.7143001T= , CM000681.1:g.7143001T=	GRCh37
NC_000019.8:g.7094001T=	NCBI36
NG_008852.2:g.156011A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2368A= MANE Select	ENSP00000303830.4:p.Thr790=
ENST00000302850.9:c.2368A=	ENSP00000303830.4:p.Thr790=
ENST00000341500.9:c.2332A=	ENSP00000342838.4:p.Thr778=
ENST00000597211.1:n.51A=
NM_000208.2:c.2368A=	NP_000199.2:p.Thr790=
NM_000208.3:c.2368A=	NP_000199.2:p.Thr790=
NM_001079817.1:c.2332A=	NP_001073285.1:p.Thr778=
NM_001079817.2:c.2332A=	NP_001073285.1:p.Thr778=
XM_011527988.1:c.2446A=	XP_011526290.1:p.Thr816=
XM_011527989.1:c.2410A=	XP_011526291.1:p.Thr804=
XM_011527988.2:c.2368A=	XP_011526290.2:p.Thr790=
XM_011527989.3:c.2332A=	XP_011526291.2:p.Thr778=
NM_000208.4:c.2368A= MANE Select	NP_000199.2:p.Thr790=
NM_001079817.3:c.2332A=	NP_001073285.1:p.Thr778=