Canonical Allele Identifier: CA2320775579

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7141764G= , CM000681.2:g.7141764G=	GRCh38
NC_000019.9:g.7141775G= , CM000681.1:g.7141775G=	GRCh37
NC_000019.8:g.7092775G=	NCBI36
NG_008852.2:g.157237C=

Transcript Alleles

HGVS	Amino-acid Change
NM_000208.4:c.2595C= MANE Select	NP_000199.2:p.Asn865=
ENST00000302850.10:c.2595C= MANE Select	ENSP00000303830.4:p.Asn865=
NM_000208.2:c.2595C=	NP_000199.2:p.Asn865=
NM_000208.3:c.2595C=	NP_000199.2:p.Asn865=
NM_001079817.1:c.2559C=	NP_001073285.1:p.Asn853=
NM_001079817.2:c.2559C=	NP_001073285.1:p.Asn853=
NM_001079817.3:c.2559C=	NP_001073285.1:p.Asn853=
ENST00000302850.9:c.2595C=	ENSP00000303830.4:p.Asn865=
ENST00000341500.9:c.2559C=	ENSP00000342838.4:p.Asn853=
ENST00000597211.1:n.278C=
XM_011527988.1:c.2673C=	XP_011526290.1:p.Asn891=
XM_011527988.2:c.2595C=	XP_011526290.2:p.Asn865=
XM_011527989.1:c.2637C=	XP_011526291.1:p.Asn879=
XM_011527989.3:c.2559C=	XP_011526291.2:p.Asn853=