Canonical Allele Identifier: CA2320766380

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7122662C= , CM000681.2:g.7122662C=	GRCh38
NC_000019.9:g.7122673C= , CM000681.1:g.7122673C=	GRCh37
NC_000019.8:g.7073673C=	NCBI36
NG_008852.2:g.176339G=

Transcript Alleles

HGVS	Amino-acid Change
NM_000208.4:c.3481G= MANE Select	NP_000199.2:p.Ala1161=
ENST00000302850.10:c.3481G= MANE Select	ENSP00000303830.4:p.Ala1161=
NM_000208.2:c.3481G=	NP_000199.2:p.Ala1161=
NM_000208.3:c.3481G=	NP_000199.2:p.Ala1161=
NM_001079817.1:c.3445G=	NP_001073285.1:p.Ala1149=
NM_001079817.2:c.3445G=	NP_001073285.1:p.Ala1149=
NM_001079817.3:c.3445G=	NP_001073285.1:p.Ala1149=
ENST00000302850.9:c.3481G=	ENSP00000303830.4:p.Ala1161=
ENST00000341500.9:c.3445G=	ENSP00000342838.4:p.Ala1149=
ENST00000593970.1:n.327G=
ENST00000601099.1:n.392G=
XM_011527988.1:c.3556G=	XP_011526290.1:p.Ala1186=
XM_011527988.2:c.3478G=	XP_011526290.2:p.Ala1160=
XM_011527989.1:c.3520G=	XP_011526291.1:p.Ala1174=
XM_011527989.3:c.3442G=	XP_011526291.2:p.Ala1148=