Canonical Allele Identifier: CA2320771108

Gene: INSR

Genomic Alleles

HGVS	Genome Assembly
NC_000019.10:g.7132303G= , CM000681.2:g.7132303G=	GRCh38
NC_000019.9:g.7132314G= , CM000681.1:g.7132314G=	GRCh37
NC_000019.8:g.7083314G=	NCBI36
NG_008852.2:g.166698C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000302850.10:c.2697C= MANE Select	ENSP00000303830.4:p.Cys899=
ENST00000302850.9:c.2697C=	ENSP00000303830.4:p.Cys899=
ENST00000341500.9:c.2661C=	ENSP00000342838.4:p.Cys887=
NM_000208.2:c.2697C=	NP_000199.2:p.Cys899=
NM_000208.3:c.2697C=	NP_000199.2:p.Cys899=
NM_001079817.1:c.2661C=	NP_001073285.1:p.Cys887=
NM_001079817.2:c.2661C=	NP_001073285.1:p.Cys887=
XM_011527988.1:c.2775C=	XP_011526290.1:p.Cys925=
XM_011527989.1:c.2739C=	XP_011526291.1:p.Cys913=
XM_011527988.2:c.2697C=	XP_011526290.2:p.Cys899=
XM_011527989.3:c.2661C=	XP_011526291.2:p.Cys887=
NM_000208.4:c.2697C= MANE Select	NP_000199.2:p.Cys899=
NM_001079817.3:c.2661C=	NP_001073285.1:p.Cys887=