Canonical Allele Identifier: CA2320763727

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117262C= , CM000681.2:g.7117262C=	GRCh38
NC_000019.9:g.7117273C= , CM000681.1:g.7117273C=	GRCh37
NC_000019.8:g.7068273C=	NCBI36
NG_008852.2:g.181739G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3943G= MANE Select	ENSP00000303830.4:p.Glu1315=
ENST00000302850.9:c.3943G=	ENSP00000303830.4:p.Glu1315=
ENST00000341500.9:c.3907G=	ENSP00000342838.4:p.Glu1303=
NM_000208.2:c.3943G=	NP_000199.2:p.Glu1315=
NM_000208.3:c.3943G=	NP_000199.2:p.Glu1315=
NM_001079817.1:c.3907G=	NP_001073285.1:p.Glu1303=
NM_001079817.2:c.3907G=	NP_001073285.1:p.Glu1303=
XM_011527988.1:c.4018G=	XP_011526290.1:p.Glu1340=
XM_011527989.1:c.3982G=	XP_011526291.1:p.Glu1328=
XM_011527988.2:c.3940G=	XP_011526290.2:p.Glu1314=
XM_011527989.3:c.3904G=	XP_011526291.2:p.Glu1302=
NM_000208.4:c.3943G= MANE Select	NP_000199.2:p.Glu1315=
NM_001079817.3:c.3907G=	NP_001073285.1:p.Glu1303=