Canonical Allele Identifier: CA2320763965

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117071C= , CM000681.2:g.7117071C=	GRCh38
NC_000019.9:g.7117082C= , CM000681.1:g.7117082C=	GRCh37
NC_000019.8:g.7068082C=	NCBI36
NG_008852.2:g.181930G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4134G= MANE Select	ENSP00000303830.4:p.Arg1378=
ENST00000302850.9:c.4134G=	ENSP00000303830.4:p.Arg1378=
ENST00000341500.9:c.4098G=	ENSP00000342838.4:p.Arg1366=
NM_000208.2:c.4134G=	NP_000199.2:p.Arg1378=
NM_000208.3:c.4134G=	NP_000199.2:p.Arg1378=
NM_001079817.1:c.4098G=	NP_001073285.1:p.Arg1366=
NM_001079817.2:c.4098G=	NP_001073285.1:p.Arg1366=
XM_011527988.1:c.4209G=	XP_011526290.1:p.Arg1403=
XM_011527989.1:c.4173G=	XP_011526291.1:p.Arg1391=
XM_011527988.2:c.4131G=	XP_011526290.2:p.Arg1377=
XM_011527989.3:c.4095G=	XP_011526291.2:p.Arg1365=
NM_000208.4:c.4134G= MANE Select	NP_000199.2:p.Arg1378=
NM_001079817.3:c.4098G=	NP_001073285.1:p.Arg1366=