Canonical Allele Identifier: CA2320763699

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117200A= , CM000681.2:g.7117200A=	GRCh38
NC_000019.9:g.7117211A= , CM000681.1:g.7117211A=	GRCh37
NC_000019.8:g.7068211A=	NCBI36
NG_008852.2:g.181801T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4005T= MANE Select	ENSP00000303830.4:p.Cys1335=
ENST00000302850.9:c.4005T=	ENSP00000303830.4:p.Cys1335=
ENST00000341500.9:c.3969T=	ENSP00000342838.4:p.Cys1323=
NM_000208.2:c.4005T=	NP_000199.2:p.Cys1335=
NM_000208.3:c.4005T=	NP_000199.2:p.Cys1335=
NM_001079817.1:c.3969T=	NP_001073285.1:p.Cys1323=
NM_001079817.2:c.3969T=	NP_001073285.1:p.Cys1323=
XM_011527988.1:c.4080T=	XP_011526290.1:p.Cys1360=
XM_011527989.1:c.4044T=	XP_011526291.1:p.Cys1348=
XM_011527988.2:c.4002T=	XP_011526290.2:p.Cys1334=
XM_011527989.3:c.3966T=	XP_011526291.2:p.Cys1322=
NM_000208.4:c.4005T= MANE Select	NP_000199.2:p.Cys1335=
NM_001079817.3:c.3969T=	NP_001073285.1:p.Cys1323=