Canonical Allele Identifier: CA2320775558

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7141695A= , CM000681.2:g.7141695A=	GRCh38
NC_000019.9:g.7141706A= , CM000681.1:g.7141706A=	GRCh37
NC_000019.8:g.7092706A=	NCBI36
NG_008852.2:g.157306T=

Transcript Alleles

HGVS	Amino-acid change
ENST00000302850.10:c.2664T= MANE Select	ENSP00000303830.4:p.Tyr888=
ENST00000302850.9:c.2664T=	ENSP00000303830.4:p.Tyr888=
ENST00000341500.9:c.2628T=	ENSP00000342838.4:p.Tyr876=
ENST00000597211.1:n.347T=
NM_000208.2:c.2664T=	NP_000199.2:p.Tyr888=
NM_000208.3:c.2664T=	NP_000199.2:p.Tyr888=
NM_001079817.1:c.2628T=	NP_001073285.1:p.Tyr876=
NM_001079817.2:c.2628T=	NP_001073285.1:p.Tyr876=
XM_011527988.1:c.2742T=	XP_011526290.1:p.Tyr914=
XM_011527989.1:c.2706T=	XP_011526291.1:p.Tyr902=
XM_011527988.2:c.2664T=	XP_011526290.2:p.Tyr888=
XM_011527989.3:c.2628T=	XP_011526291.2:p.Tyr876=
NM_000208.4:c.2664T= MANE Select	NP_000199.2:p.Tyr888=
NM_001079817.3:c.2628T=	NP_001073285.1:p.Tyr876=