Canonical Allele Identifier: CA2320767952

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125403G= , CM000681.2:g.7125403G=	GRCh38
NC_000019.9:g.7125414G= , CM000681.1:g.7125414G=	GRCh37
NC_000019.8:g.7076414G=	NCBI36
NG_008852.2:g.173598C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3138C= MANE Select	ENSP00000303830.4:p.Ile1046=
ENST00000302850.9:c.3138C=	ENSP00000303830.4:p.Ile1046=
ENST00000341500.9:c.3102C=	ENSP00000342838.4:p.Ile1034=
NM_000208.2:c.3138C=	NP_000199.2:p.Ile1046=
NM_000208.3:c.3138C=	NP_000199.2:p.Ile1046=
NM_001079817.1:c.3102C=	NP_001073285.1:p.Ile1034=
NM_001079817.2:c.3102C=	NP_001073285.1:p.Ile1034=
XM_011527988.1:c.3213C=	XP_011526290.1:p.Ile1071=
XM_011527989.1:c.3177C=	XP_011526291.1:p.Ile1059=
XM_011527988.2:c.3135C=	XP_011526290.2:p.Ile1045=
XM_011527989.3:c.3099C=	XP_011526291.2:p.Ile1033=
NM_000208.4:c.3138C= MANE Select	NP_000199.2:p.Ile1046=
NM_001079817.3:c.3102C=	NP_001073285.1:p.Ile1034=