Canonical Allele Identifier: CA2320771048

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132155T= , CM000681.2:g.7132155T=	GRCh38
NC_000019.9:g.7132166T= , CM000681.1:g.7132166T=	GRCh37
NC_000019.8:g.7083166T=	NCBI36
NG_008852.2:g.166846A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2842+3A= MANE Select	ENSP00000303830.4:n.2842+3A=
ENST00000302850.9:c.2842+3A=	ENSP00000303830.4:n.2842+3A=
ENST00000341500.9:c.2806+3A=	ENSP00000342838.4:n.2806+3A=
NM_000208.2:c.2842+3A=	NP_000199.2:n.2842+3A=
NM_000208.3:c.2842+3A=	NP_000199.2:n.2842+3A=
NM_001079817.1:c.2806+3A=	NP_001073285.1:n.2806+3A=
NM_001079817.2:c.2806+3A=	NP_001073285.1:n.2806+3A=
XM_011527988.1:c.2920+3A=	XP_011526290.1:n.2920+3A=
XM_011527989.1:c.2884+3A=	XP_011526291.1:n.2884+3A=
XM_011527988.2:c.2842+3A=	XP_011526290.2:n.2842+3A=
XM_011527989.3:c.2806+3A=	XP_011526291.2:n.2806+3A=
NM_000208.4:c.2842+3A= MANE Select	NP_000199.2:n.2842+3A=
NM_001079817.3:c.2806+3A=	NP_001073285.1:n.2806+3A=