Canonical Allele Identifier: CA2320767909

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125299A= , CM000681.2:g.7125299A=	GRCh38
NC_000019.9:g.7125310A= , CM000681.1:g.7125310A=	GRCh37
NC_000019.8:g.7076310A=	NCBI36
NG_008852.2:g.173702T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3242T= MANE Select	ENSP00000303830.4:p.Phe1081=
ENST00000302850.9:c.3242T=	ENSP00000303830.4:p.Phe1081=
ENST00000341500.9:c.3206T=	ENSP00000342838.4:p.Phe1069=
ENST00000593970.1:n.88T=
NM_000208.2:c.3242T=	NP_000199.2:p.Phe1081=
NM_000208.3:c.3242T=	NP_000199.2:p.Phe1081=
NM_001079817.1:c.3206T=	NP_001073285.1:p.Phe1069=
NM_001079817.2:c.3206T=	NP_001073285.1:p.Phe1069=
XM_011527988.1:c.3317T=	XP_011526290.1:p.Phe1106=
XM_011527989.1:c.3281T=	XP_011526291.1:p.Phe1094=
XM_011527988.2:c.3239T=	XP_011526290.2:p.Phe1080=
XM_011527989.3:c.3203T=	XP_011526291.2:p.Phe1068=
NM_000208.4:c.3242T= MANE Select	NP_000199.2:p.Phe1081=
NM_001079817.3:c.3206T=	NP_001073285.1:p.Phe1069=