Canonical Allele Identifier: CA2320769443

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128826C= , CM000681.2:g.7128826C=	GRCh38
NC_000019.9:g.7128837C= , CM000681.1:g.7128837C=	GRCh37
NC_000019.8:g.7079837C=	NCBI36
NG_008852.2:g.170175G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2945+26G= MANE Select	ENSP00000303830.4:n.2945+26G=
ENST00000302850.9:c.2945+26G=	ENSP00000303830.4:n.2945+26G=
ENST00000341500.9:c.2909+26G=	ENSP00000342838.4:n.2909+26G=
NM_000208.2:c.2945+26G=	NP_000199.2:n.2945+26G=
NM_000208.3:c.2945+26G=	NP_000199.2:n.2945+26G=
NM_001079817.1:c.2909+26G=	NP_001073285.1:n.2909+26G=
NM_001079817.2:c.2909+26G=	NP_001073285.1:n.2909+26G=
XM_011527988.1:c.3020+26G=	XP_011526290.1:n.3020+26G=
XM_011527989.1:c.2984+26G=	XP_011526291.1:n.2984+26G=
XM_011527988.2:c.2942+26G=	XP_011526290.2:n.2942+26G=
XM_011527989.3:c.2906+26G=	XP_011526291.2:n.2906+26G=
NM_000208.4:c.2945+26G= MANE Select	NP_000199.2:n.2945+26G=
NM_001079817.3:c.2909+26G=	NP_001073285.1:n.2909+26G=