Canonical Allele Identifier: CA1237128850

Gene: KIDINS220

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.8731443T= , CM000664.2:g.8731443T=	GRCh38
NC_000002.11:g.8871573T= , CM000664.1:g.8871573T=	GRCh37
NC_000002.10:g.8789024T=	NCBI36
NG_053168.1:g.111197A=

Transcript Alleles

HGVS	Amino-acid Change
ENST00000685097.1:c.4296A=	ENSP00000510510.1:p.Ser1432=
ENST00000686383.1:n.4478A=
ENST00000686906.1:c.*481A=	ENSP00000508907.1:n.*481A=
ENST00000687894.1:c.*1965A=	ENSP00000509577.1:n.*1965A=
ENST00000687912.1:c.4098A=	ENSP00000508455.1:p.Ser1366=
ENST00000689369.1:c.3882+2001A=	ENSP00000509856.1:n.3882+2001A=
ENST00000689852.1:c.3915+2001A=	ENSP00000510537.1:n.3915+2001A=
ENST00000691030.1:c.4572A=	ENSP00000510148.1:p.Ser1524=
ENST00000693394.1:c.3882+2001A=	ENSP00000509014.1:n.3882+2001A=
ENST00000693432.1:c.4053+2001A=	ENSP00000510486.1:n.4053+2001A=
ENST00000693597.1:n.861+2001A=
ENST00000256707.8:c.4593A= MANE Select	ENSP00000256707.4:p.Ser1531=
ENST00000569008.2:c.3882+2001A=	ENSP00000491461.1:n.3882+2001A=
ENST00000256707.7:c.4593A=	ENSP00000256707.3:p.Ser1531=
ENST00000473731.5:c.4536A=	ENSP00000418974.1:p.Ser1512=
ENST00000488729.5:c.*4482A=	ENSP00000417390.1:n.*4482A=
ENST00000496383.5:c.3123+2001A=	ENSP00000420364.1:n.3123+2001A=
NM_020738.2:c.4593A=	NP_065789.1:p.Ser1531=
NM_001348729.1:c.4596A=	NP_001335658.1:p.Ser1532=
NM_001348731.1:c.4539A=	NP_001335660.1:p.Ser1513=
NM_001348732.1:c.4536A=	NP_001335661.1:p.Ser1512=
NM_001348734.1:c.4425A=	NP_001335663.1:p.Ser1475=
NM_001348735.1:c.4422A=	NP_001335664.1:p.Ser1474=
NM_001348736.1:c.4296A=	NP_001335665.1:p.Ser1432=
NM_001348738.1:c.3996+2001A=	NP_001335667.1:n.3996+2001A=
NM_001348739.1:c.3885+2001A=	NP_001335668.1:n.3885+2001A=
NM_001348740.1:c.3885+2001A=	NP_001335669.1:n.3885+2001A=
NM_001348741.1:c.3882+2001A=	NP_001335670.1:n.3882+2001A=
NM_001348742.1:c.3882+2001A=	NP_001335671.1:n.3882+2001A=
NM_001348743.1:c.3882+2001A=	NP_001335672.1:n.3882+2001A=
NM_020738.3:c.4593A=	NP_065789.1:p.Ser1531=
NR_145964.1:n.4252+2001A=
NR_145965.1:n.4078+2001A=
NM_001348729.2:c.4596A=	NP_001335658.1:p.Ser1532=
NM_001348731.2:c.4539A=	NP_001335660.1:p.Ser1513=
NM_001348732.2:c.4536A=	NP_001335661.1:p.Ser1512=
NM_001348734.2:c.4425A=	NP_001335663.1:p.Ser1475=
NM_001348735.2:c.4422A=	NP_001335664.1:p.Ser1474=
NM_001348736.2:c.4296A=	NP_001335665.1:p.Ser1432=
NM_001348738.2:c.3996+2001A=	NP_001335667.1:n.3996+2001A=
NM_001348739.2:c.3885+2001A=	NP_001335668.1:n.3885+2001A=
NM_001348740.2:c.3885+2001A=	NP_001335669.1:n.3885+2001A=
NM_001348741.2:c.3882+2001A=	NP_001335670.1:n.3882+2001A=
NM_001348742.2:c.3882+2001A=	NP_001335671.1:n.3882+2001A=
NM_001348743.2:c.3882+2001A=	NP_001335672.1:n.3882+2001A=
NM_020738.4:c.4593A= MANE Select	NP_065789.1:p.Ser1531=
NR_145964.2:n.4226+2001A=
NR_145965.2:n.4052+2001A=