Canonical Allele Identifier: CA2320763714

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117228T= , CM000681.2:g.7117228T=	GRCh38
NC_000019.9:g.7117239T= , CM000681.1:g.7117239T=	GRCh37
NC_000019.8:g.7068239T=	NCBI36
NG_008852.2:g.181773A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3977A= MANE Select	ENSP00000303830.4:p.Asn1326=
ENST00000302850.9:c.3977A=	ENSP00000303830.4:p.Asn1326=
ENST00000341500.9:c.3941A=	ENSP00000342838.4:p.Asn1314=
NM_000208.2:c.3977A=	NP_000199.2:p.Asn1326=
NM_000208.3:c.3977A=	NP_000199.2:p.Asn1326=
NM_001079817.1:c.3941A=	NP_001073285.1:p.Asn1314=
NM_001079817.2:c.3941A=	NP_001073285.1:p.Asn1314=
XM_011527988.1:c.4052A=	XP_011526290.1:p.Asn1351=
XM_011527989.1:c.4016A=	XP_011526291.1:p.Asn1339=
XM_011527988.2:c.3974A=	XP_011526290.2:p.Asn1325=
XM_011527989.3:c.3938A=	XP_011526291.2:p.Asn1313=
NM_000208.4:c.3977A= MANE Select	NP_000199.2:p.Asn1326=
NM_001079817.3:c.3941A=	NP_001073285.1:p.Asn1314=