Canonical Allele Identifier: CA2320788250

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7166273C= , CM000681.2:g.7166273C=	GRCh38
NC_000019.9:g.7166284C= , CM000681.1:g.7166284C=	GRCh37
NC_000019.8:g.7117284C=	NCBI36
NG_008852.2:g.132728G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.1742G= MANE Select	ENSP00000303830.4:p.Arg581=
ENST00000302850.9:c.1742G=	ENSP00000303830.4:p.Arg581=
ENST00000341500.9:c.1742G=	ENSP00000342838.4:p.Arg581=
ENST00000598216.1:n.1717G=
ENST00000600492.1:c.143G=	ENSP00000473170.1:p.Arg48=
NM_000208.2:c.1742G=	NP_000199.2:p.Arg581=
NM_000208.3:c.1742G=	NP_000199.2:p.Arg581=
NM_001079817.1:c.1742G=	NP_001073285.1:p.Arg581=
NM_001079817.2:c.1742G=	NP_001073285.1:p.Arg581=
XM_011527988.1:c.1820G=	XP_011526290.1:p.Arg607=
XM_011527989.1:c.1820G=	XP_011526291.1:p.Arg607=
XM_011527988.2:c.1742G=	XP_011526290.2:p.Arg581=
XM_011527989.3:c.1742G=	XP_011526291.2:p.Arg581=
NM_000208.4:c.1742G= MANE Select	NP_000199.2:p.Arg581=
NM_001079817.3:c.1742G=	NP_001073285.1:p.Arg581=