Canonical Allele Identifier: CA2320763689

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117178G= , CM000681.2:g.7117178G=	GRCh38
NC_000019.9:g.7117189G= , CM000681.1:g.7117189G=	GRCh37
NC_000019.8:g.7068189G=	NCBI36
NG_008852.2:g.181823C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4027C= MANE Select	ENSP00000303830.4:p.Arg1343=
ENST00000302850.9:c.4027C=	ENSP00000303830.4:p.Arg1343=
ENST00000341500.9:c.3991C=	ENSP00000342838.4:p.Arg1331=
NM_000208.2:c.4027C=	NP_000199.2:p.Arg1343=
NM_000208.3:c.4027C=	NP_000199.2:p.Arg1343=
NM_001079817.1:c.3991C=	NP_001073285.1:p.Arg1331=
NM_001079817.2:c.3991C=	NP_001073285.1:p.Arg1331=
XM_011527988.1:c.4102C=	XP_011526290.1:p.Arg1368=
XM_011527989.1:c.4066C=	XP_011526291.1:p.Arg1356=
XM_011527988.2:c.4024C=	XP_011526290.2:p.Arg1342=
XM_011527989.3:c.3988C=	XP_011526291.2:p.Arg1330=
NM_000208.4:c.4027C= MANE Select	NP_000199.2:p.Arg1343=
NM_001079817.3:c.3991C=	NP_001073285.1:p.Arg1331=