Canonical Allele Identifier: CA2320763947

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117060G= , CM000681.2:g.7117060G=	GRCh38
NC_000019.9:g.7117071G= , CM000681.1:g.7117071G=	GRCh37
NC_000019.8:g.7068071G=	NCBI36
NG_008852.2:g.181941C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4145C= MANE Select	ENSP00000303830.4:p.Ser1382=
ENST00000302850.9:c.4145C=	ENSP00000303830.4:p.Ser1382=
ENST00000341500.9:c.4109C=	ENSP00000342838.4:p.Ser1370=
NM_000208.2:c.4145C=	NP_000199.2:p.Ser1382=
NM_000208.3:c.4145C=	NP_000199.2:p.Ser1382=
NM_001079817.1:c.4109C=	NP_001073285.1:p.Ser1370=
NM_001079817.2:c.4109C=	NP_001073285.1:p.Ser1370=
XM_011527988.1:c.4220C=	XP_011526290.1:p.Ser1407=
XM_011527989.1:c.4184C=	XP_011526291.1:p.Ser1395=
XM_011527988.2:c.4142C=	XP_011526290.2:p.Ser1381=
XM_011527989.3:c.4106C=	XP_011526291.2:p.Ser1369=
NM_000208.4:c.4145C= MANE Select	NP_000199.2:p.Ser1382=
NM_001079817.3:c.4109C=	NP_001073285.1:p.Ser1370=