Canonical Allele Identifier: CA2320764858

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7119576C= , CM000681.2:g.7119576C=	GRCh38
NC_000019.9:g.7119587C= , CM000681.1:g.7119587C=	GRCh37
NC_000019.8:g.7070587C=	NCBI36
NG_008852.2:g.179425G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.3667G= MANE Select	ENSP00000303830.4:p.Gly1223=
ENST00000302850.9:c.3667G=	ENSP00000303830.4:p.Gly1223=
ENST00000341500.9:c.3631G=	ENSP00000342838.4:p.Gly1211=
NM_000208.2:c.3667G=	NP_000199.2:p.Gly1223=
NM_000208.3:c.3667G=	NP_000199.2:p.Gly1223=
NM_001079817.1:c.3631G=	NP_001073285.1:p.Gly1211=
NM_001079817.2:c.3631G=	NP_001073285.1:p.Gly1211=
XM_011527988.1:c.3742G=	XP_011526290.1:p.Gly1248=
XM_011527989.1:c.3706G=	XP_011526291.1:p.Gly1236=
XM_011527988.2:c.3664G=	XP_011526290.2:p.Gly1222=
XM_011527989.3:c.3628G=	XP_011526291.2:p.Gly1210=
NM_000208.4:c.3667G= MANE Select	NP_000199.2:p.Gly1223=
NM_001079817.3:c.3631G=	NP_001073285.1:p.Gly1211=