Canonical Allele Identifier: CA2320763956

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7117068G= , CM000681.2:g.7117068G=	GRCh38
NC_000019.9:g.7117079G= , CM000681.1:g.7117079G=	GRCh37
NC_000019.8:g.7068079G=	NCBI36
NG_008852.2:g.181933C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.4137C= MANE Select	ENSP00000303830.4:p.Ser1379=
ENST00000302850.9:c.4137C=	ENSP00000303830.4:p.Ser1379=
ENST00000341500.9:c.4101C=	ENSP00000342838.4:p.Ser1367=
NM_000208.2:c.4137C=	NP_000199.2:p.Ser1379=
NM_000208.3:c.4137C=	NP_000199.2:p.Ser1379=
NM_001079817.1:c.4101C=	NP_001073285.1:p.Ser1367=
NM_001079817.2:c.4101C=	NP_001073285.1:p.Ser1367=
XM_011527988.1:c.4212C=	XP_011526290.1:p.Ser1404=
XM_011527989.1:c.4176C=	XP_011526291.1:p.Ser1392=
XM_011527988.2:c.4134C=	XP_011526290.2:p.Ser1378=
XM_011527989.3:c.4098C=	XP_011526291.2:p.Ser1366=
NM_000208.4:c.4137C= MANE Select	NP_000199.2:p.Ser1379=
NM_001079817.3:c.4101C=	NP_001073285.1:p.Ser1367=