Canonical Allele Identifier: CA2320769462

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7128869A= , CM000681.2:g.7128869A=	GRCh38
NC_000019.9:g.7128880A= , CM000681.1:g.7128880A=	GRCh37
NC_000019.8:g.7079880A=	NCBI36
NG_008852.2:g.170132T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2928T= MANE Select	ENSP00000303830.4:p.Tyr976=
ENST00000302850.9:c.2928T=	ENSP00000303830.4:p.Tyr976=
ENST00000341500.9:c.2892T=	ENSP00000342838.4:p.Tyr964=
NM_000208.2:c.2928T=	NP_000199.2:p.Tyr976=
NM_000208.3:c.2928T=	NP_000199.2:p.Tyr976=
NM_001079817.1:c.2892T=	NP_001073285.1:p.Tyr964=
NM_001079817.2:c.2892T=	NP_001073285.1:p.Tyr964=
XM_011527988.1:c.3003T=	XP_011526290.1:p.Tyr1001=
XM_011527989.1:c.2967T=	XP_011526291.1:p.Tyr989=
XM_011527988.2:c.2925T=	XP_011526290.2:p.Tyr975=
XM_011527989.3:c.2889T=	XP_011526291.2:p.Tyr963=
NM_000208.4:c.2928T= MANE Select	NP_000199.2:p.Tyr976=
NM_001079817.3:c.2892T=	NP_001073285.1:p.Tyr964=