Canonical Allele Identifier: CA2320771112

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132317C= , CM000681.2:g.7132317C=	GRCh38
NC_000019.9:g.7132328C= , CM000681.1:g.7132328C=	GRCh37
NC_000019.8:g.7083328C=	NCBI36
NG_008852.2:g.166684G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2683G= MANE Select	ENSP00000303830.4:p.Glu895=
ENST00000302850.9:c.2683G=	ENSP00000303830.4:p.Glu895=
ENST00000341500.9:c.2647G=	ENSP00000342838.4:p.Glu883=
NM_000208.2:c.2683G=	NP_000199.2:p.Glu895=
NM_000208.3:c.2683G=	NP_000199.2:p.Glu895=
NM_001079817.1:c.2647G=	NP_001073285.1:p.Glu883=
NM_001079817.2:c.2647G=	NP_001073285.1:p.Glu883=
XM_011527988.1:c.2761G=	XP_011526290.1:p.Glu921=
XM_011527989.1:c.2725G=	XP_011526291.1:p.Glu909=
XM_011527988.2:c.2683G=	XP_011526290.2:p.Glu895=
XM_011527989.3:c.2647G=	XP_011526291.2:p.Glu883=
NM_000208.4:c.2683G= MANE Select	NP_000199.2:p.Glu895=
NM_001079817.3:c.2647G=	NP_001073285.1:p.Glu883=