Canonical Allele Identifier: CA2320767933

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125355T= , CM000681.2:g.7125355T=	GRCh38
NC_000019.9:g.7125366T= , CM000681.1:g.7125366T=	GRCh37
NC_000019.8:g.7076366T=	NCBI36
NG_008852.2:g.173646A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3186A= MANE Select	ENSP00000303830.4:p.Ser1062=
ENST00000302850.9:c.3186A=	ENSP00000303830.4:p.Ser1062=
ENST00000341500.9:c.3150A=	ENSP00000342838.4:p.Ser1050=
ENST00000593970.1:n.32A=
NM_000208.2:c.3186A=	NP_000199.2:p.Ser1062=
NM_000208.3:c.3186A=	NP_000199.2:p.Ser1062=
NM_001079817.1:c.3150A=	NP_001073285.1:p.Ser1050=
NM_001079817.2:c.3150A=	NP_001073285.1:p.Ser1050=
XM_011527988.1:c.3261A=	XP_011526290.1:p.Ser1087=
XM_011527989.1:c.3225A=	XP_011526291.1:p.Ser1075=
XM_011527988.2:c.3183A=	XP_011526290.2:p.Ser1061=
XM_011527989.3:c.3147A=	XP_011526291.2:p.Ser1049=
NM_000208.4:c.3186A= MANE Select	NP_000199.2:p.Ser1062=
NM_001079817.3:c.3150A=	NP_001073285.1:p.Ser1050=