Canonical Allele Identifier: CA612608926
Gene: IRS2 HGNC NCBI

Linked Data

dbSNP Id: rs1175148154

Genomic Alleles

HGVS Genome Assembly
NC_000013.11:g.109767142del , CM000675.2:g.109767142del GRCh38
NC_000013.10:g.110419489del , CM000675.1:g.110419489del GRCh37
NC_000013.9:g.109217490del NCBI36
NG_008154.1:g.24427del

Transcript Alleles

HGVS Amino-acid Change
ENST00000375856.5:c.4013-10833del MANE Select ENSP00000365016.3:n.4013-10833del
ENST00000375856.4:c.4013-10833del ENSP00000365016.3:n.4013-10833del
NM_003749.2:c.4013-10833del NP_003740.2:n.4013-10833del
NM_003749.3:c.4013-10833del MANE Select NP_003740.2:n.4013-10833del