Canonical Allele Identifier: CA2320763696

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117187C= , CM000681.2:g.7117187C=	GRCh38
NC_000019.9:g.7117198C= , CM000681.1:g.7117198C=	GRCh37
NC_000019.8:g.7068198C=	NCBI36
NG_008852.2:g.181814G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4018G= MANE Select	ENSP00000303830.4:p.Ala1340=
ENST00000302850.9:c.4018G=	ENSP00000303830.4:p.Ala1340=
ENST00000341500.9:c.3982G=	ENSP00000342838.4:p.Ala1328=
NM_000208.2:c.4018G=	NP_000199.2:p.Ala1340=
NM_000208.3:c.4018G=	NP_000199.2:p.Ala1340=
NM_001079817.1:c.3982G=	NP_001073285.1:p.Ala1328=
NM_001079817.2:c.3982G=	NP_001073285.1:p.Ala1328=
XM_011527988.1:c.4093G=	XP_011526290.1:p.Ala1365=
XM_011527989.1:c.4057G=	XP_011526291.1:p.Ala1353=
XM_011527988.2:c.4015G=	XP_011526290.2:p.Ala1339=
XM_011527989.3:c.3979G=	XP_011526291.2:p.Ala1327=
NM_000208.4:c.4018G= MANE Select	NP_000199.2:p.Ala1340=
NM_001079817.3:c.3982G=	NP_001073285.1:p.Ala1328=