Canonical Allele Identifier: CA2320767966

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125439G= , CM000681.2:g.7125439G=	GRCh38
NC_000019.9:g.7125450G= , CM000681.1:g.7125450G=	GRCh37
NC_000019.8:g.7076450G=	NCBI36
NG_008852.2:g.173562C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3102C= MANE Select	ENSP00000303830.4:p.Phe1034=
ENST00000302850.9:c.3102C=	ENSP00000303830.4:p.Phe1034=
ENST00000341500.9:c.3066C=	ENSP00000342838.4:p.Phe1022=
NM_000208.2:c.3102C=	NP_000199.2:p.Phe1034=
NM_000208.3:c.3102C=	NP_000199.2:p.Phe1034=
NM_001079817.1:c.3066C=	NP_001073285.1:p.Phe1022=
NM_001079817.2:c.3066C=	NP_001073285.1:p.Phe1022=
XM_011527988.1:c.3177C=	XP_011526290.1:p.Phe1059=
XM_011527989.1:c.3141C=	XP_011526291.1:p.Phe1047=
XM_011527988.2:c.3099C=	XP_011526290.2:p.Phe1033=
XM_011527989.3:c.3063C=	XP_011526291.2:p.Phe1021=
NM_000208.4:c.3102C= MANE Select	NP_000199.2:p.Phe1034=
NM_001079817.3:c.3066C=	NP_001073285.1:p.Phe1022=