Canonical Allele Identifier: CA2320763738

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117278G= , CM000681.2:g.7117278G=	GRCh38
NC_000019.9:g.7117289G= , CM000681.1:g.7117289G=	GRCh37
NC_000019.8:g.7068289G=	NCBI36
NG_008852.2:g.181723C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3927C= MANE Select	ENSP00000303830.4:p.Asn1309=
ENST00000302850.9:c.3927C=	ENSP00000303830.4:p.Asn1309=
ENST00000341500.9:c.3891C=	ENSP00000342838.4:p.Asn1297=
NM_000208.2:c.3927C=	NP_000199.2:p.Asn1309=
NM_000208.3:c.3927C=	NP_000199.2:p.Asn1309=
NM_001079817.1:c.3891C=	NP_001073285.1:p.Asn1297=
NM_001079817.2:c.3891C=	NP_001073285.1:p.Asn1297=
XM_011527988.1:c.4002C=	XP_011526290.1:p.Asn1334=
XM_011527989.1:c.3966C=	XP_011526291.1:p.Asn1322=
XM_011527988.2:c.3924C=	XP_011526290.2:p.Asn1308=
XM_011527989.3:c.3888C=	XP_011526291.2:p.Asn1296=
NM_000208.4:c.3927C= MANE Select	NP_000199.2:p.Asn1309=
NM_001079817.3:c.3891C=	NP_001073285.1:p.Asn1297=