Canonical Allele Identifier: CA2320765515

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7120650T= , CM000681.2:g.7120650T=	GRCh38
NC_000019.9:g.7120661T= , CM000681.1:g.7120661T=	GRCh37
NC_000019.8:g.7071661T=	NCBI36
NG_008852.2:g.178351A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3629A= MANE Select	ENSP00000303830.4:p.Asp1210=
ENST00000302850.9:c.3629A=	ENSP00000303830.4:p.Asp1210=
ENST00000341500.9:c.3593A=	ENSP00000342838.4:p.Asp1198=
ENST00000601099.1:n.540A=
NM_000208.2:c.3629A=	NP_000199.2:p.Asp1210=
NM_000208.3:c.3629A=	NP_000199.2:p.Asp1210=
NM_001079817.1:c.3593A=	NP_001073285.1:p.Asp1198=
NM_001079817.2:c.3593A=	NP_001073285.1:p.Asp1198=
XM_011527988.1:c.3704A=	XP_011526290.1:p.Asp1235=
XM_011527989.1:c.3668A=	XP_011526291.1:p.Asp1223=
XM_011527988.2:c.3626A=	XP_011526290.2:p.Asp1209=
XM_011527989.3:c.3590A=	XP_011526291.2:p.Asp1197=
NM_000208.4:c.3629A= MANE Select	NP_000199.2:p.Asp1210=
NM_001079817.3:c.3593A=	NP_001073285.1:p.Asp1198=