Canonical Allele Identifier: CA2320769455

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128853T= , CM000681.2:g.7128853T=	GRCh38
NC_000019.9:g.7128864T= , CM000681.1:g.7128864T=	GRCh37
NC_000019.8:g.7079864T=	NCBI36
NG_008852.2:g.170148A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2944A= MANE Select	ENSP00000303830.4:p.Arg982=
ENST00000302850.9:c.2944A=	ENSP00000303830.4:p.Arg982=
ENST00000341500.9:c.2908A=	ENSP00000342838.4:p.Arg970=
NM_000208.2:c.2944A=	NP_000199.2:p.Arg982=
NM_000208.3:c.2944A=	NP_000199.2:p.Arg982=
NM_001079817.1:c.2908A=	NP_001073285.1:p.Arg970=
NM_001079817.2:c.2908A=	NP_001073285.1:p.Arg970=
XM_011527988.1:c.3019A=	XP_011526290.1:p.Arg1007=
XM_011527989.1:c.2983A=	XP_011526291.1:p.Arg995=
XM_011527988.2:c.2941A=	XP_011526290.2:p.Arg981=
XM_011527989.3:c.2905A=	XP_011526291.2:p.Arg969=
NM_000208.4:c.2944A= MANE Select	NP_000199.2:p.Arg982=
NM_001079817.3:c.2908A=	NP_001073285.1:p.Arg970=