Canonical Allele Identifier: CA2320763786

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117329G= , CM000681.2:g.7117329G=	GRCh38
NC_000019.9:g.7117340G= , CM000681.1:g.7117340G=	GRCh37
NC_000019.8:g.7068340G=	NCBI36
NG_008852.2:g.181672C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3876C= MANE Select	ENSP00000303830.4:p.Asp1292=
ENST00000302850.9:c.3876C=	ENSP00000303830.4:p.Asp1292=
ENST00000341500.9:c.3840C=	ENSP00000342838.4:p.Asp1280=
NM_000208.2:c.3876C=	NP_000199.2:p.Asp1292=
NM_000208.3:c.3876C=	NP_000199.2:p.Asp1292=
NM_001079817.1:c.3840C=	NP_001073285.1:p.Asp1280=
NM_001079817.2:c.3840C=	NP_001073285.1:p.Asp1280=
XM_011527988.1:c.3951C=	XP_011526290.1:p.Asp1317=
XM_011527989.1:c.3915C=	XP_011526291.1:p.Asp1305=
XM_011527988.2:c.3873C=	XP_011526290.2:p.Asp1291=
XM_011527989.3:c.3837C=	XP_011526291.2:p.Asp1279=
NM_000208.4:c.3876C= MANE Select	NP_000199.2:p.Asp1292=
NM_001079817.3:c.3840C=	NP_001073285.1:p.Asp1280=