Canonical Allele Identifier: CA2118539345

Gene: IRS2

Genomic Alleles

HGVS	Genome Assembly
NC_000013.11:g.109767143A= , CM000675.2:g.109767143A=	GRCh38
NC_000013.10:g.110419490A= , CM000675.1:g.110419490A=	GRCh37
NC_000013.9:g.109217491A=	NCBI36
NG_008154.1:g.24425T=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000375856.5:c.4013-10835T= MANE Select	ENSP00000365016.3:n.4013-10835T=
ENST00000375856.4:c.4013-10835T=	ENSP00000365016.3:n.4013-10835T=
NM_003749.2:c.4013-10835T=	NP_003740.2:n.4013-10835T=
NM_003749.3:c.4013-10835T= MANE Select	NP_003740.2:n.4013-10835T=