Canonical Allele Identifier: CA2320763708

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117213C= , CM000681.2:g.7117213C=	GRCh38
NC_000019.9:g.7117224C= , CM000681.1:g.7117224C=	GRCh37
NC_000019.8:g.7068224C=	NCBI36
NG_008852.2:g.181788G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3992G= MANE Select	ENSP00000303830.4:p.Arg1331=
ENST00000302850.9:c.3992G=	ENSP00000303830.4:p.Arg1331=
ENST00000341500.9:c.3956G=	ENSP00000342838.4:p.Arg1319=
NM_000208.2:c.3992G=	NP_000199.2:p.Arg1331=
NM_000208.3:c.3992G=	NP_000199.2:p.Arg1331=
NM_001079817.1:c.3956G=	NP_001073285.1:p.Arg1319=
NM_001079817.2:c.3956G=	NP_001073285.1:p.Arg1319=
XM_011527988.1:c.4067G=	XP_011526290.1:p.Arg1356=
XM_011527989.1:c.4031G=	XP_011526291.1:p.Arg1344=
XM_011527988.2:c.3989G=	XP_011526290.2:p.Arg1330=
XM_011527989.3:c.3953G=	XP_011526291.2:p.Arg1318=
NM_000208.4:c.3992G= MANE Select	NP_000199.2:p.Arg1331=
NM_001079817.3:c.3956G=	NP_001073285.1:p.Arg1319=