Canonical Allele Identifier: CA2320767971

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125461C= , CM000681.2:g.7125461C=	GRCh38
NC_000019.9:g.7125472C= , CM000681.1:g.7125472C=	GRCh37
NC_000019.8:g.7076472C=	NCBI36
NG_008852.2:g.173540G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3080G= MANE Select	ENSP00000303830.4:p.Arg1027=
ENST00000302850.9:c.3080G=	ENSP00000303830.4:p.Arg1027=
ENST00000341500.9:c.3044G=	ENSP00000342838.4:p.Arg1015=
NM_000208.2:c.3080G=	NP_000199.2:p.Arg1027=
NM_000208.3:c.3080G=	NP_000199.2:p.Arg1027=
NM_001079817.1:c.3044G=	NP_001073285.1:p.Arg1015=
NM_001079817.2:c.3044G=	NP_001073285.1:p.Arg1015=
XM_011527988.1:c.3155G=	XP_011526290.1:p.Arg1052=
XM_011527989.1:c.3119G=	XP_011526291.1:p.Arg1040=
XM_011527988.2:c.3077G=	XP_011526290.2:p.Arg1026=
XM_011527989.3:c.3041G=	XP_011526291.2:p.Arg1014=
NM_000208.4:c.3080G= MANE Select	NP_000199.2:p.Arg1027=
NM_001079817.3:c.3044G=	NP_001073285.1:p.Arg1015=