Canonical Allele Identifier: CA10489729

Gene: IRS4

Genomic Alleles

HGVS	Genome Assembly
NC_000023.11:g.108734580dup , CM000685.2:g.108734580dup	GRCh38
NC_000023.10:g.107977810dup , CM000685.1:g.107977810dup	GRCh37
NC_000023.9:g.107864466dup	NCBI36
NG_013239.1:g.6805dup

Transcript Alleles

HGVS	Amino-acid Change
NM_001379150.1:c.1772dup MANE Select	NP_001366079.1:p.Lys592GlnfsTer12
ENST00000372129.4:c.1772dup MANE Select	ENSP00000361202.3:p.Lys592GlnfsTer12
NM_003604.2:c.1772dup	NP_003595.1:p.Lys592GlnfsTer12
ENST00000372129.3:c.1772dup	ENSP00000361202.2:p.Lys592GlnfsTer12
ENST00000564206.2:c.1772dup	ENSP00000505547.1:p.Lys592GlnfsTer12
XM_005262220.2:c.1772dup	XP_005262277.1:p.Lys592GlnfsTer12
XM_006724713.2:c.1772dup	XP_006724776.1:p.Lys592GlnfsTer12
XM_006724713.3:c.1772dup	XP_006724776.1:p.Lys592GlnfsTer12
XM_011531061.1:c.1772dup	XP_011529363.1:p.Lys592GlnfsTer12