Canonical Allele Identifier: CA2320765523

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120677C= , CM000681.2:g.7120677C=	GRCh38
NC_000019.9:g.7120688C= , CM000681.1:g.7120688C=	GRCh37
NC_000019.8:g.7071688C=	NCBI36
NG_008852.2:g.178324G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000208.4:c.3602G= MANE Select	NP_000199.2:p.Arg1201=
ENST00000302850.10:c.3602G= MANE Select	ENSP00000303830.4:p.Arg1201=
NM_000208.2:c.3602G=	NP_000199.2:p.Arg1201=
NM_000208.3:c.3602G=	NP_000199.2:p.Arg1201=
NM_001079817.1:c.3566G=	NP_001073285.1:p.Arg1189=
NM_001079817.2:c.3566G=	NP_001073285.1:p.Arg1189=
NM_001079817.3:c.3566G=	NP_001073285.1:p.Arg1189=
ENST00000302850.9:c.3602G=	ENSP00000303830.4:p.Arg1201=
ENST00000341500.9:c.3566G=	ENSP00000342838.4:p.Arg1189=
ENST00000601099.1:n.513G=
XM_011527988.1:c.3677G=	XP_011526290.1:p.Arg1226=
XM_011527988.2:c.3599G=	XP_011526290.2:p.Arg1200=
XM_011527989.1:c.3641G=	XP_011526291.1:p.Arg1214=
XM_011527989.3:c.3563G=	XP_011526291.2:p.Arg1188=