Canonical Allele Identifier: CA2320767937

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7125366C= , CM000681.2:g.7125366C=	GRCh38
NC_000019.9:g.7125377C= , CM000681.1:g.7125377C=	GRCh37
NC_000019.8:g.7076377C=	NCBI36
NG_008852.2:g.173635G=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3175G= MANE Select	ENSP00000303830.4:p.Val1059=
ENST00000302850.9:c.3175G=	ENSP00000303830.4:p.Val1059=
ENST00000341500.9:c.3139G=	ENSP00000342838.4:p.Val1047=
ENST00000593970.1:n.21G=
NM_000208.2:c.3175G=	NP_000199.2:p.Val1059=
NM_000208.3:c.3175G=	NP_000199.2:p.Val1059=
NM_001079817.1:c.3139G=	NP_001073285.1:p.Val1047=
NM_001079817.2:c.3139G=	NP_001073285.1:p.Val1047=
XM_011527988.1:c.3250G=	XP_011526290.1:p.Val1084=
XM_011527989.1:c.3214G=	XP_011526291.1:p.Val1072=
XM_011527988.2:c.3172G=	XP_011526290.2:p.Val1058=
XM_011527989.3:c.3136G=	XP_011526291.2:p.Val1046=
NM_000208.4:c.3175G= MANE Select	NP_000199.2:p.Val1059=
NM_001079817.3:c.3139G=	NP_001073285.1:p.Val1047=