Canonical Allele Identifier: CA2320763722

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117247C= , CM000681.2:g.7117247C=	GRCh38
NC_000019.9:g.7117258C= , CM000681.1:g.7117258C=	GRCh37
NC_000019.8:g.7068258C=	NCBI36
NG_008852.2:g.181754G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3958G= MANE Select	ENSP00000303830.4:p.Glu1320=
ENST00000302850.9:c.3958G=	ENSP00000303830.4:p.Glu1320=
ENST00000341500.9:c.3922G=	ENSP00000342838.4:p.Glu1308=
NM_000208.2:c.3958G=	NP_000199.2:p.Glu1320=
NM_000208.3:c.3958G=	NP_000199.2:p.Glu1320=
NM_001079817.1:c.3922G=	NP_001073285.1:p.Glu1308=
NM_001079817.2:c.3922G=	NP_001073285.1:p.Glu1308=
XM_011527988.1:c.4033G=	XP_011526290.1:p.Glu1345=
XM_011527989.1:c.3997G=	XP_011526291.1:p.Glu1333=
XM_011527988.2:c.3955G=	XP_011526290.2:p.Glu1319=
XM_011527989.3:c.3919G=	XP_011526291.2:p.Glu1307=
NM_000208.4:c.3958G= MANE Select	NP_000199.2:p.Glu1320=
NM_001079817.3:c.3922G=	NP_001073285.1:p.Glu1308=