Canonical Allele Identifier: CA2576669110

Gene: KIDINS220

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.8731410_8731413del , CM000664.2:g.8731410_8731413del	GRCh38
NC_000002.11:g.8871540_8871543del , CM000664.1:g.8871540_8871543del	GRCh37
NC_000002.10:g.8788991_8788994del	NCBI36
NG_053168.1:g.111230_111233del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685097.1:c.4329_4332del	ENSP00000510510.1:p.Asp1443GlufsTer7
ENST00000686383.1:n.4511_4514del
ENST00000686906.1:c.*514_*517del	ENSP00000508907.1:n.*514_*517del
ENST00000687894.1:c.*1998_*2001del	ENSP00000509577.1:n.*1998_*2001del
ENST00000687912.1:c.4131_4134del	ENSP00000508455.1:p.Asp1377GlufsTer7
ENST00000689369.1:c.3882+2034_3882+2037del	ENSP00000509856.1:n.3882+2034_3882+2037del
ENST00000689852.1:c.3915+2034_3915+2037del	ENSP00000510537.1:n.3915+2034_3915+2037del
ENST00000691030.1:c.4605_4608del	ENSP00000510148.1:p.Asp1535GlufsTer7
ENST00000693394.1:c.3882+2034_3882+2037del	ENSP00000509014.1:n.3882+2034_3882+2037del
ENST00000693432.1:c.4053+2034_4053+2037del	ENSP00000510486.1:n.4053+2034_4053+2037del
ENST00000693597.1:n.861+2034_861+2037del
ENST00000256707.8:c.4626_4629del MANE Select	ENSP00000256707.4:p.Asp1542GlufsTer7
ENST00000569008.2:c.3882+2034_3882+2037del	ENSP00000491461.1:n.3882+2034_3882+2037del
ENST00000256707.7:c.4626_4629del	ENSP00000256707.3:p.Asp1542GlufsTer7
ENST00000473731.5:c.4569_4572del	ENSP00000418974.1:p.Asp1523GlufsTer7
ENST00000488729.5:c.*4515_*4518del	ENSP00000417390.1:n.*4515_*4518del
ENST00000496383.5:c.3123+2034_3123+2037del	ENSP00000420364.1:n.3123+2034_3123+2037del
NM_020738.2:c.4626_4629del	NP_065789.1:p.Asp1542GlufsTer7
NM_001348729.1:c.4629_4632del	NP_001335658.1:p.Asp1543GlufsTer7
NM_001348731.1:c.4572_4575del	NP_001335660.1:p.Asp1524GlufsTer7
NM_001348732.1:c.4569_4572del	NP_001335661.1:p.Asp1523GlufsTer7
NM_001348734.1:c.4458_4461del	NP_001335663.1:p.Asp1486GlufsTer7
NM_001348735.1:c.4455_4458del	NP_001335664.1:p.Asp1485GlufsTer7
NM_001348736.1:c.4329_4332del	NP_001335665.1:p.Asp1443GlufsTer7
NM_001348738.1:c.3996+2034_3996+2037del	NP_001335667.1:n.3996+2034_3996+2037del
NM_001348739.1:c.3885+2034_3885+2037del	NP_001335668.1:n.3885+2034_3885+2037del
NM_001348740.1:c.3885+2034_3885+2037del	NP_001335669.1:n.3885+2034_3885+2037del
NM_001348741.1:c.3882+2034_3882+2037del	NP_001335670.1:n.3882+2034_3882+2037del
NM_001348742.1:c.3882+2034_3882+2037del	NP_001335671.1:n.3882+2034_3882+2037del
NM_001348743.1:c.3882+2034_3882+2037del	NP_001335672.1:n.3882+2034_3882+2037del
NM_020738.3:c.4626_4629del	NP_065789.1:p.Asp1542GlufsTer7
NR_145964.1:n.4252+2034_4252+2037del
NR_145965.1:n.4078+2034_4078+2037del
NM_001348729.2:c.4629_4632del	NP_001335658.1:p.Asp1543GlufsTer7
NM_001348731.2:c.4572_4575del	NP_001335660.1:p.Asp1524GlufsTer7
NM_001348732.2:c.4569_4572del	NP_001335661.1:p.Asp1523GlufsTer7
NM_001348734.2:c.4458_4461del	NP_001335663.1:p.Asp1486GlufsTer7
NM_001348735.2:c.4455_4458del	NP_001335664.1:p.Asp1485GlufsTer7
NM_001348736.2:c.4329_4332del	NP_001335665.1:p.Asp1443GlufsTer7
NM_001348738.2:c.3996+2034_3996+2037del	NP_001335667.1:n.3996+2034_3996+2037del
NM_001348739.2:c.3885+2034_3885+2037del	NP_001335668.1:n.3885+2034_3885+2037del
NM_001348740.2:c.3885+2034_3885+2037del	NP_001335669.1:n.3885+2034_3885+2037del
NM_001348741.2:c.3882+2034_3882+2037del	NP_001335670.1:n.3882+2034_3882+2037del
NM_001348742.2:c.3882+2034_3882+2037del	NP_001335671.1:n.3882+2034_3882+2037del
NM_001348743.2:c.3882+2034_3882+2037del	NP_001335672.1:n.3882+2034_3882+2037del
NM_020738.4:c.4626_4629del MANE Select	NP_065789.1:p.Asp1542GlufsTer7
NR_145964.2:n.4226+2034_4226+2037del
NR_145965.2:n.4052+2034_4052+2037del