Canonical Allele Identifier: CA2320763720

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117236G= , CM000681.2:g.7117236G=	GRCh38
NC_000019.9:g.7117247G= , CM000681.1:g.7117247G=	GRCh37
NC_000019.8:g.7068247G=	NCBI36
NG_008852.2:g.181765C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3969C= MANE Select	ENSP00000303830.4:p.Asp1323=
ENST00000302850.9:c.3969C=	ENSP00000303830.4:p.Asp1323=
ENST00000341500.9:c.3933C=	ENSP00000342838.4:p.Asp1311=
NM_000208.2:c.3969C=	NP_000199.2:p.Asp1323=
NM_000208.3:c.3969C=	NP_000199.2:p.Asp1323=
NM_001079817.1:c.3933C=	NP_001073285.1:p.Asp1311=
NM_001079817.2:c.3933C=	NP_001073285.1:p.Asp1311=
XM_011527988.1:c.4044C=	XP_011526290.1:p.Asp1348=
XM_011527989.1:c.4008C=	XP_011526291.1:p.Asp1336=
XM_011527988.2:c.3966C=	XP_011526290.2:p.Asp1322=
XM_011527989.3:c.3930C=	XP_011526291.2:p.Asp1310=
NM_000208.4:c.3969C= MANE Select	NP_000199.2:p.Asp1323=
NM_001079817.3:c.3933C=	NP_001073285.1:p.Asp1311=