Canonical Allele Identifier: CA2320767902

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125283C= , CM000681.2:g.7125283C=	GRCh38
NC_000019.9:g.7125294C= , CM000681.1:g.7125294C=	GRCh37
NC_000019.8:g.7076294C=	NCBI36
NG_008852.2:g.173718G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3258G= MANE Select	ENSP00000303830.4:p.Val1086=
ENST00000302850.9:c.3258G=	ENSP00000303830.4:p.Val1086=
ENST00000341500.9:c.3222G=	ENSP00000342838.4:p.Val1074=
ENST00000593970.1:n.104G=
NM_000208.2:c.3258G=	NP_000199.2:p.Val1086=
NM_000208.3:c.3258G=	NP_000199.2:p.Val1086=
NM_001079817.1:c.3222G=	NP_001073285.1:p.Val1074=
NM_001079817.2:c.3222G=	NP_001073285.1:p.Val1074=
XM_011527988.1:c.3333G=	XP_011526290.1:p.Val1111=
XM_011527989.1:c.3297G=	XP_011526291.1:p.Val1099=
XM_011527988.2:c.3255G=	XP_011526290.2:p.Val1085=
XM_011527989.3:c.3219G=	XP_011526291.2:p.Val1073=
NM_000208.4:c.3258G= MANE Select	NP_000199.2:p.Val1086=
NM_001079817.3:c.3222G=	NP_001073285.1:p.Val1074=