Canonical Allele Identifier: CA16043967
Gene: KIDINS220 HGNC NCBI

Linked Data

ClinVar Variation Id: 374908
ClinVar RCV Id: RCV000415590
dbSNP Id: rs1057519300

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.8733447C>T , CM000664.2:g.8733447C>T GRCh38
NC_000002.11:g.8873577C>T , CM000664.1:g.8873577C>T GRCh37
NC_000002.10:g.8791028C>T NCBI36
NG_053168.1:g.109193G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000471685.2:n.1506G>A
ENST00000685097.1:c.3753G>A ENSP00000510510.1:p.Trp1251Ter
ENST00000686383.1:n.3935G>A
ENST00000686906.1:c.3850+29G>A ENSP00000508907.1:n.3850+29G>A
ENST00000687894.1:c.*1422G>A ENSP00000509577.1:n.*1422G>A
ENST00000687912.1:c.3555G>A ENSP00000508455.1:p.Trp1185Ter
ENST00000689369.1:c.3879G>A ENSP00000509856.1:p.Trp1293Ter
ENST00000689852.1:c.3912G>A ENSP00000510537.1:p.Trp1304Ter
ENST00000691030.1:c.4029G>A ENSP00000510148.1:p.Trp1343Ter
ENST00000693394.1:c.3879G>A ENSP00000509014.1:p.Trp1293Ter
ENST00000693432.1:c.4050G>A ENSP00000510486.1:p.Trp1350Ter
ENST00000693597.1:n.858G>A
ENST00000256707.8:c.4050G>A MANE Select ENSP00000256707.4:p.Trp1350Ter
ENST00000569008.2:c.3879G>A ENSP00000491461.1:p.Trp1293Ter
ENST00000256707.7:c.4050G>A ENSP00000256707.3:p.Trp1350Ter
ENST00000473731.5:c.3993G>A ENSP00000418974.1:p.Trp1331Ter
ENST00000488729.5:c.*3939G>A ENSP00000417390.1:n.*3939G>A
ENST00000489024.5:c.3882G>A ENSP00000419964.1:p.Trp1294Ter
ENST00000496383.5:c.3120G>A ENSP00000420364.1:p.Trp1040Ter
NM_020738.2:c.4050G>A NP_065789.1:p.Trp1350Ter
NM_001348729.1:c.4053G>A NP_001335658.1:p.Trp1351Ter
NM_001348731.1:c.3996G>A NP_001335660.1:p.Trp1332Ter
NM_001348732.1:c.3993G>A NP_001335661.1:p.Trp1331Ter
NM_001348734.1:c.3882G>A NP_001335663.1:p.Trp1294Ter
NM_001348735.1:c.3879G>A NP_001335664.1:p.Trp1293Ter
NM_001348736.1:c.3753G>A NP_001335665.1:p.Trp1251Ter
NM_001348738.1:c.3993G>A NP_001335667.1:p.Trp1331Ter
NM_001348739.1:c.3882G>A NP_001335668.1:p.Trp1294Ter
NM_001348740.1:c.3882G>A NP_001335669.1:p.Trp1294Ter
NM_001348741.1:c.3879G>A NP_001335670.1:p.Trp1293Ter
NM_001348742.1:c.3879G>A NP_001335671.1:p.Trp1293Ter
NM_001348743.1:c.3879G>A NP_001335672.1:p.Trp1293Ter
NM_020738.3:c.4050G>A NP_065789.1:p.Trp1350Ter
NR_145964.1:n.4249G>A
NR_145965.1:n.4075G>A
NM_001348729.2:c.4053G>A NP_001335658.1:p.Trp1351Ter
NM_001348731.2:c.3996G>A NP_001335660.1:p.Trp1332Ter
NM_001348732.2:c.3993G>A NP_001335661.1:p.Trp1331Ter
NM_001348734.2:c.3882G>A NP_001335663.1:p.Trp1294Ter
NM_001348735.2:c.3879G>A NP_001335664.1:p.Trp1293Ter
NM_001348736.2:c.3753G>A NP_001335665.1:p.Trp1251Ter
NM_001348738.2:c.3993G>A NP_001335667.1:p.Trp1331Ter
NM_001348739.2:c.3882G>A NP_001335668.1:p.Trp1294Ter
NM_001348740.2:c.3882G>A NP_001335669.1:p.Trp1294Ter
NM_001348741.2:c.3879G>A NP_001335670.1:p.Trp1293Ter
NM_001348742.2:c.3879G>A NP_001335671.1:p.Trp1293Ter
NM_001348743.2:c.3879G>A NP_001335672.1:p.Trp1293Ter
NM_020738.4:c.4050G>A MANE Select NP_065789.1:p.Trp1350Ter
NR_145964.2:n.4223G>A
NR_145965.2:n.4049G>A