Canonical Allele Identifier: CA2320764017

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117104G= , CM000681.2:g.7117104G=	GRCh38
NC_000019.9:g.7117115G= , CM000681.1:g.7117115G=	GRCh37
NC_000019.8:g.7068115G=	NCBI36
NG_008852.2:g.181897C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4101C= MANE Select	ENSP00000303830.4:p.Gly1367=
ENST00000302850.9:c.4101C=	ENSP00000303830.4:p.Gly1367=
ENST00000341500.9:c.4065C=	ENSP00000342838.4:p.Gly1355=
NM_000208.2:c.4101C=	NP_000199.2:p.Gly1367=
NM_000208.3:c.4101C=	NP_000199.2:p.Gly1367=
NM_001079817.1:c.4065C=	NP_001073285.1:p.Gly1355=
NM_001079817.2:c.4065C=	NP_001073285.1:p.Gly1355=
XM_011527988.1:c.4176C=	XP_011526290.1:p.Gly1392=
XM_011527989.1:c.4140C=	XP_011526291.1:p.Gly1380=
XM_011527988.2:c.4098C=	XP_011526290.2:p.Gly1366=
XM_011527989.3:c.4062C=	XP_011526291.2:p.Gly1354=
NM_000208.4:c.4101C= MANE Select	NP_000199.2:p.Gly1367=
NM_001079817.3:c.4065C=	NP_001073285.1:p.Gly1355=