Canonical Allele Identifier: CA2320763755

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117293G= , CM000681.2:g.7117293G=	GRCh38
NC_000019.9:g.7117304G= , CM000681.1:g.7117304G=	GRCh37
NC_000019.8:g.7068304G=	NCBI36
NG_008852.2:g.181708C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.3912C= MANE Select	ENSP00000303830.4:p.Phe1304=
ENST00000302850.9:c.3912C=	ENSP00000303830.4:p.Phe1304=
ENST00000341500.9:c.3876C=	ENSP00000342838.4:p.Phe1292=
NM_000208.2:c.3912C=	NP_000199.2:p.Phe1304=
NM_000208.3:c.3912C=	NP_000199.2:p.Phe1304=
NM_001079817.1:c.3876C=	NP_001073285.1:p.Phe1292=
NM_001079817.2:c.3876C=	NP_001073285.1:p.Phe1292=
XM_011527988.1:c.3987C=	XP_011526290.1:p.Phe1329=
XM_011527989.1:c.3951C=	XP_011526291.1:p.Phe1317=
XM_011527988.2:c.3909C=	XP_011526290.2:p.Phe1303=
XM_011527989.3:c.3873C=	XP_011526291.2:p.Phe1291=
NM_000208.4:c.3912C= MANE Select	NP_000199.2:p.Phe1304=
NM_001079817.3:c.3876C=	NP_001073285.1:p.Phe1292=