Canonical Allele Identifier: CA2320776129

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7143065C= , CM000681.2:g.7143065C=	GRCh38
NC_000019.9:g.7143076C= , CM000681.1:g.7143076C=	GRCh37
NC_000019.8:g.7094076C=	NCBI36
NG_008852.2:g.155936G=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2293G= MANE Select	ENSP00000303830.4:p.Gly765=
ENST00000302850.9:c.2293G=	ENSP00000303830.4:p.Gly765=
ENST00000341500.9:c.2257G=	ENSP00000342838.4:p.Gly753=
NM_000208.2:c.2293G=	NP_000199.2:p.Gly765=
NM_000208.3:c.2293G=	NP_000199.2:p.Gly765=
NM_001079817.1:c.2257G=	NP_001073285.1:p.Gly753=
NM_001079817.2:c.2257G=	NP_001073285.1:p.Gly753=
XM_011527988.1:c.2371G=	XP_011526290.1:p.Gly791=
XM_011527989.1:c.2335G=	XP_011526291.1:p.Gly779=
XM_011527988.2:c.2293G=	XP_011526290.2:p.Gly765=
XM_011527989.3:c.2257G=	XP_011526291.2:p.Gly753=
NM_000208.4:c.2293G= MANE Select	NP_000199.2:p.Gly765=
NM_001079817.3:c.2257G=	NP_001073285.1:p.Gly753=