Canonical Allele Identifier: CA2320771060

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132186T= , CM000681.2:g.7132186T=	GRCh38
NC_000019.9:g.7132197T= , CM000681.1:g.7132197T=	GRCh37
NC_000019.8:g.7083197T=	NCBI36
NG_008852.2:g.166815A=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2814A= MANE Select	ENSP00000303830.4:p.Glu938=
ENST00000302850.9:c.2814A=	ENSP00000303830.4:p.Glu938=
ENST00000341500.9:c.2778A=	ENSP00000342838.4:p.Glu926=
NM_000208.2:c.2814A=	NP_000199.2:p.Glu938=
NM_000208.3:c.2814A=	NP_000199.2:p.Glu938=
NM_001079817.1:c.2778A=	NP_001073285.1:p.Glu926=
NM_001079817.2:c.2778A=	NP_001073285.1:p.Glu926=
XM_011527988.1:c.2892A=	XP_011526290.1:p.Glu964=
XM_011527989.1:c.2856A=	XP_011526291.1:p.Glu952=
XM_011527988.2:c.2814A=	XP_011526290.2:p.Glu938=
XM_011527989.3:c.2778A=	XP_011526291.2:p.Glu926=
NM_000208.4:c.2814A= MANE Select	NP_000199.2:p.Glu938=
NM_001079817.3:c.2778A=	NP_001073285.1:p.Glu926=