Canonical Allele Identifier: CA2320763703

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117207G= , CM000681.2:g.7117207G=	GRCh38
NC_000019.9:g.7117218G= , CM000681.1:g.7117218G=	GRCh37
NC_000019.8:g.7068218G=	NCBI36
NG_008852.2:g.181794C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3998C= MANE Select	ENSP00000303830.4:p.Ser1333=
ENST00000302850.9:c.3998C=	ENSP00000303830.4:p.Ser1333=
ENST00000341500.9:c.3962C=	ENSP00000342838.4:p.Ser1321=
NM_000208.2:c.3998C=	NP_000199.2:p.Ser1333=
NM_000208.3:c.3998C=	NP_000199.2:p.Ser1333=
NM_001079817.1:c.3962C=	NP_001073285.1:p.Ser1321=
NM_001079817.2:c.3962C=	NP_001073285.1:p.Ser1321=
XM_011527988.1:c.4073C=	XP_011526290.1:p.Ser1358=
XM_011527989.1:c.4037C=	XP_011526291.1:p.Ser1346=
XM_011527988.2:c.3995C=	XP_011526290.2:p.Ser1332=
XM_011527989.3:c.3959C=	XP_011526291.2:p.Ser1320=
NM_000208.4:c.3998C= MANE Select	NP_000199.2:p.Ser1333=
NM_001079817.3:c.3962C=	NP_001073285.1:p.Ser1321=