Canonical Allele Identifier: CA2320767970

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125458T= , CM000681.2:g.7125458T=	GRCh38
NC_000019.9:g.7125469T= , CM000681.1:g.7125469T=	GRCh37
NC_000019.8:g.7076469T=	NCBI36
NG_008852.2:g.173543A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3083A= MANE Select	ENSP00000303830.4:p.Glu1028=
ENST00000302850.9:c.3083A=	ENSP00000303830.4:p.Glu1028=
ENST00000341500.9:c.3047A=	ENSP00000342838.4:p.Glu1016=
NM_000208.2:c.3083A=	NP_000199.2:p.Glu1028=
NM_000208.3:c.3083A=	NP_000199.2:p.Glu1028=
NM_001079817.1:c.3047A=	NP_001073285.1:p.Glu1016=
NM_001079817.2:c.3047A=	NP_001073285.1:p.Glu1016=
XM_011527988.1:c.3158A=	XP_011526290.1:p.Glu1053=
XM_011527989.1:c.3122A=	XP_011526291.1:p.Glu1041=
XM_011527988.2:c.3080A=	XP_011526290.2:p.Glu1027=
XM_011527989.3:c.3044A=	XP_011526291.2:p.Glu1015=
NM_000208.4:c.3083A= MANE Select	NP_000199.2:p.Glu1028=
NM_001079817.3:c.3047A=	NP_001073285.1:p.Glu1016=