Canonical Allele Identifier: CA1237128858
Gene: KIDINS220 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000002.12:g.8731477G= , CM000664.2:g.8731477G= GRCh38
NC_000002.11:g.8871607G= , CM000664.1:g.8871607G= GRCh37
NC_000002.10:g.8789058G= NCBI36
NG_053168.1:g.111163C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000685097.1:c.4262C= ENSP00000510510.1:p.Pro1421=
ENST00000686383.1:n.4444C=
ENST00000686906.1:c.*447C= ENSP00000508907.1:n.*447C=
ENST00000687894.1:c.*1931C= ENSP00000509577.1:n.*1931C=
ENST00000687912.1:c.4064C= ENSP00000508455.1:p.Pro1355=
ENST00000689369.1:c.3882+1967C= ENSP00000509856.1:n.3882+1967C=
ENST00000689852.1:c.3915+1967C= ENSP00000510537.1:n.3915+1967C=
ENST00000691030.1:c.4538C= ENSP00000510148.1:p.Pro1513=
ENST00000693394.1:c.3882+1967C= ENSP00000509014.1:n.3882+1967C=
ENST00000693432.1:c.4053+1967C= ENSP00000510486.1:n.4053+1967C=
ENST00000693597.1:n.861+1967C=
ENST00000256707.8:c.4559C= MANE Select ENSP00000256707.4:p.Pro1520=
ENST00000569008.2:c.3882+1967C= ENSP00000491461.1:n.3882+1967C=
ENST00000256707.7:c.4559C= ENSP00000256707.3:p.Pro1520=
ENST00000473731.5:c.4502C= ENSP00000418974.1:p.Pro1501=
ENST00000488729.5:c.*4448C= ENSP00000417390.1:n.*4448C=
ENST00000496383.5:c.3123+1967C= ENSP00000420364.1:n.3123+1967C=
NM_020738.2:c.4559C= NP_065789.1:p.Pro1520=
NM_001348729.1:c.4562C= NP_001335658.1:p.Pro1521=
NM_001348731.1:c.4505C= NP_001335660.1:p.Pro1502=
NM_001348732.1:c.4502C= NP_001335661.1:p.Pro1501=
NM_001348734.1:c.4391C= NP_001335663.1:p.Pro1464=
NM_001348735.1:c.4388C= NP_001335664.1:p.Pro1463=
NM_001348736.1:c.4262C= NP_001335665.1:p.Pro1421=
NM_001348738.1:c.3996+1967C= NP_001335667.1:n.3996+1967C=
NM_001348739.1:c.3885+1967C= NP_001335668.1:n.3885+1967C=
NM_001348740.1:c.3885+1967C= NP_001335669.1:n.3885+1967C=
NM_001348741.1:c.3882+1967C= NP_001335670.1:n.3882+1967C=
NM_001348742.1:c.3882+1967C= NP_001335671.1:n.3882+1967C=
NM_001348743.1:c.3882+1967C= NP_001335672.1:n.3882+1967C=
NM_020738.3:c.4559C= NP_065789.1:p.Pro1520=
NR_145964.1:n.4252+1967C=
NR_145965.1:n.4078+1967C=
NM_001348729.2:c.4562C= NP_001335658.1:p.Pro1521=
NM_001348731.2:c.4505C= NP_001335660.1:p.Pro1502=
NM_001348732.2:c.4502C= NP_001335661.1:p.Pro1501=
NM_001348734.2:c.4391C= NP_001335663.1:p.Pro1464=
NM_001348735.2:c.4388C= NP_001335664.1:p.Pro1463=
NM_001348736.2:c.4262C= NP_001335665.1:p.Pro1421=
NM_001348738.2:c.3996+1967C= NP_001335667.1:n.3996+1967C=
NM_001348739.2:c.3885+1967C= NP_001335668.1:n.3885+1967C=
NM_001348740.2:c.3885+1967C= NP_001335669.1:n.3885+1967C=
NM_001348741.2:c.3882+1967C= NP_001335670.1:n.3882+1967C=
NM_001348742.2:c.3882+1967C= NP_001335671.1:n.3882+1967C=
NM_001348743.2:c.3882+1967C= NP_001335672.1:n.3882+1967C=
NM_020738.4:c.4559C= MANE Select NP_065789.1:p.Pro1520=
NR_145964.2:n.4226+1967C=
NR_145965.2:n.4052+1967C=