Canonical Allele Identifier: CA2320767980

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125480C= , CM000681.2:g.7125480C=	GRCh38
NC_000019.9:g.7125491C= , CM000681.1:g.7125491C=	GRCh37
NC_000019.8:g.7076491C=	NCBI36
NG_008852.2:g.173521G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3061G= MANE Select	ENSP00000303830.4:p.Glu1021=
ENST00000302850.9:c.3061G=	ENSP00000303830.4:p.Glu1021=
ENST00000341500.9:c.3025G=	ENSP00000342838.4:p.Glu1009=
NM_000208.2:c.3061G=	NP_000199.2:p.Glu1021=
NM_000208.3:c.3061G=	NP_000199.2:p.Glu1021=
NM_001079817.1:c.3025G=	NP_001073285.1:p.Glu1009=
NM_001079817.2:c.3025G=	NP_001073285.1:p.Glu1009=
XM_011527988.1:c.3136G=	XP_011526290.1:p.Glu1046=
XM_011527989.1:c.3100G=	XP_011526291.1:p.Glu1034=
XM_011527988.2:c.3058G=	XP_011526290.2:p.Glu1020=
XM_011527989.3:c.3022G=	XP_011526291.2:p.Glu1008=
NM_000208.4:c.3061G= MANE Select	NP_000199.2:p.Glu1021=
NM_001079817.3:c.3025G=	NP_001073285.1:p.Glu1009=