Canonical Allele Identifier: CA2320767955

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125412C= , CM000681.2:g.7125412C=	GRCh38
NC_000019.9:g.7125423C= , CM000681.1:g.7125423C=	GRCh37
NC_000019.8:g.7076423C=	NCBI36
NG_008852.2:g.173589G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3129G= MANE Select	ENSP00000303830.4:p.Arg1043=
ENST00000302850.9:c.3129G=	ENSP00000303830.4:p.Arg1043=
ENST00000341500.9:c.3093G=	ENSP00000342838.4:p.Arg1031=
NM_000208.2:c.3129G=	NP_000199.2:p.Arg1043=
NM_000208.3:c.3129G=	NP_000199.2:p.Arg1043=
NM_001079817.1:c.3093G=	NP_001073285.1:p.Arg1031=
NM_001079817.2:c.3093G=	NP_001073285.1:p.Arg1031=
XM_011527988.1:c.3204G=	XP_011526290.1:p.Arg1068=
XM_011527989.1:c.3168G=	XP_011526291.1:p.Arg1056=
XM_011527988.2:c.3126G=	XP_011526290.2:p.Arg1042=
XM_011527989.3:c.3090G=	XP_011526291.2:p.Arg1030=
NM_000208.4:c.3129G= MANE Select	NP_000199.2:p.Arg1043=
NM_001079817.3:c.3093G=	NP_001073285.1:p.Arg1031=