Canonical Allele Identifier: CA2320776206

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7142980T= , CM000681.2:g.7142980T=	GRCh38
NC_000019.9:g.7142991T= , CM000681.1:g.7142991T=	GRCh37
NC_000019.8:g.7093991T=	NCBI36
NG_008852.2:g.156021A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2378A= MANE Select	ENSP00000303830.4:p.Glu793=
ENST00000302850.9:c.2378A=	ENSP00000303830.4:p.Glu793=
ENST00000341500.9:c.2342A=	ENSP00000342838.4:p.Glu781=
ENST00000597211.1:n.61A=
NM_000208.2:c.2378A=	NP_000199.2:p.Glu793=
NM_000208.3:c.2378A=	NP_000199.2:p.Glu793=
NM_001079817.1:c.2342A=	NP_001073285.1:p.Glu781=
NM_001079817.2:c.2342A=	NP_001073285.1:p.Glu781=
XM_011527988.1:c.2456A=	XP_011526290.1:p.Glu819=
XM_011527989.1:c.2420A=	XP_011526291.1:p.Glu807=
XM_011527988.2:c.2378A=	XP_011526290.2:p.Glu793=
XM_011527989.3:c.2342A=	XP_011526291.2:p.Glu781=
NM_000208.4:c.2378A= MANE Select	NP_000199.2:p.Glu793=
NM_001079817.3:c.2342A=	NP_001073285.1:p.Glu781=