Canonical Allele Identifier: CA2320763735

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117273G= , CM000681.2:g.7117273G=	GRCh38
NC_000019.9:g.7117284G= , CM000681.1:g.7117284G=	GRCh37
NC_000019.8:g.7068284G=	NCBI36
NG_008852.2:g.181728C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3932C= MANE Select	ENSP00000303830.4:p.Ala1311=
ENST00000302850.9:c.3932C=	ENSP00000303830.4:p.Ala1311=
ENST00000341500.9:c.3896C=	ENSP00000342838.4:p.Ala1299=
NM_000208.2:c.3932C=	NP_000199.2:p.Ala1311=
NM_000208.3:c.3932C=	NP_000199.2:p.Ala1311=
NM_001079817.1:c.3896C=	NP_001073285.1:p.Ala1299=
NM_001079817.2:c.3896C=	NP_001073285.1:p.Ala1299=
XM_011527988.1:c.4007C=	XP_011526290.1:p.Ala1336=
XM_011527989.1:c.3971C=	XP_011526291.1:p.Ala1324=
XM_011527988.2:c.3929C=	XP_011526290.2:p.Ala1310=
XM_011527989.3:c.3893C=	XP_011526291.2:p.Ala1298=
NM_000208.4:c.3932C= MANE Select	NP_000199.2:p.Ala1311=
NM_001079817.3:c.3896C=	NP_001073285.1:p.Ala1299=