Canonical Allele Identifier: CA2320767984

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125486A= , CM000681.2:g.7125486A=	GRCh38
NC_000019.9:g.7125497A= , CM000681.1:g.7125497A=	GRCh37
NC_000019.8:g.7076497A=	NCBI36
NG_008852.2:g.173515T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3055T= MANE Select	ENSP00000303830.4:p.Ser1019=
ENST00000302850.9:c.3055T=	ENSP00000303830.4:p.Ser1019=
ENST00000341500.9:c.3019T=	ENSP00000342838.4:p.Ser1007=
NM_000208.2:c.3055T=	NP_000199.2:p.Ser1019=
NM_000208.3:c.3055T=	NP_000199.2:p.Ser1019=
NM_001079817.1:c.3019T=	NP_001073285.1:p.Ser1007=
NM_001079817.2:c.3019T=	NP_001073285.1:p.Ser1007=
XM_011527988.1:c.3130T=	XP_011526290.1:p.Ser1044=
XM_011527989.1:c.3094T=	XP_011526291.1:p.Ser1032=
XM_011527988.2:c.3052T=	XP_011526290.2:p.Ser1018=
XM_011527989.3:c.3016T=	XP_011526291.2:p.Ser1006=
NM_000208.4:c.3055T= MANE Select	NP_000199.2:p.Ser1019=
NM_001079817.3:c.3019T=	NP_001073285.1:p.Ser1007=