Canonical Allele Identifier: CA2320767989

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125498C= , CM000681.2:g.7125498C=	GRCh38
NC_000019.9:g.7125509C= , CM000681.1:g.7125509C=	GRCh37
NC_000019.8:g.7076509C=	NCBI36
NG_008852.2:g.173503G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3043G= MANE Select	ENSP00000303830.4:p.Glu1015=
ENST00000302850.9:c.3043G=	ENSP00000303830.4:p.Glu1015=
ENST00000341500.9:c.3007G=	ENSP00000342838.4:p.Glu1003=
NM_000208.2:c.3043G=	NP_000199.2:p.Glu1015=
NM_000208.3:c.3043G=	NP_000199.2:p.Glu1015=
NM_001079817.1:c.3007G=	NP_001073285.1:p.Glu1003=
NM_001079817.2:c.3007G=	NP_001073285.1:p.Glu1003=
XM_011527988.1:c.3118G=	XP_011526290.1:p.Glu1040=
XM_011527989.1:c.3082G=	XP_011526291.1:p.Glu1028=
XM_011527988.2:c.3040G=	XP_011526290.2:p.Glu1014=
XM_011527989.3:c.3004G=	XP_011526291.2:p.Glu1002=
NM_000208.4:c.3043G= MANE Select	NP_000199.2:p.Glu1015=
NM_001079817.3:c.3007G=	NP_001073285.1:p.Glu1003=