Canonical Allele Identifier: CA2118539312

Gene: IRS2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.109767073G= , CM000675.2:g.109767073G=	GRCh38
NC_000013.10:g.110419420G= , CM000675.1:g.110419420G=	GRCh37
NC_000013.9:g.109217421G=	NCBI36
NG_008154.1:g.24495C=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375856.5:c.4013-10765C= MANE Select	ENSP00000365016.3:n.4013-10765C=
ENST00000375856.4:c.4013-10765C=	ENSP00000365016.3:n.4013-10765C=
NM_003749.2:c.4013-10765C=	NP_003740.2:n.4013-10765C=
NM_003749.3:c.4013-10765C= MANE Select	NP_003740.2:n.4013-10765C=