Canonical Allele Identifier: CA425083171

Gene: KIDINS220

Linked Data

• MyVariant Identifiers: chr2:g.8871561T>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.8731431T>A , CM000664.2:g.8731431T>A	GRCh38
NC_000002.11:g.8871561T>A , CM000664.1:g.8871561T>A	GRCh37
NC_000002.10:g.8789012T>A	NCBI36
NG_053168.1:g.111209A>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000685097.1:c.4308A>T	ENSP00000510510.1:p.Pro1436=
ENST00000686383.1:n.4490A>T
ENST00000686906.1:c.*493A>T	ENSP00000508907.1:n.*493A>T
ENST00000687894.1:c.*1977A>T	ENSP00000509577.1:n.*1977A>T
ENST00000687912.1:c.4110A>T	ENSP00000508455.1:p.Pro1370=
ENST00000689369.1:c.3882+2013A>T	ENSP00000509856.1:n.3882+2013A>T
ENST00000689852.1:c.3915+2013A>T	ENSP00000510537.1:n.3915+2013A>T
ENST00000691030.1:c.4584A>T	ENSP00000510148.1:p.Pro1528=
ENST00000693394.1:c.3882+2013A>T	ENSP00000509014.1:n.3882+2013A>T
ENST00000693432.1:c.4053+2013A>T	ENSP00000510486.1:n.4053+2013A>T
ENST00000693597.1:n.861+2013A>T
ENST00000256707.8:c.4605A>T MANE Select	ENSP00000256707.4:p.Pro1535=
ENST00000569008.2:c.3882+2013A>T	ENSP00000491461.1:n.3882+2013A>T
ENST00000256707.7:c.4605A>T	ENSP00000256707.3:p.Pro1535=
ENST00000473731.5:c.4548A>T	ENSP00000418974.1:p.Pro1516=
ENST00000488729.5:c.*4494A>T	ENSP00000417390.1:n.*4494A>T
ENST00000496383.5:c.3123+2013A>T	ENSP00000420364.1:n.3123+2013A>T
NM_020738.2:c.4605A>T	NP_065789.1:p.Pro1535=
NM_001348729.1:c.4608A>T	NP_001335658.1:p.Pro1536=
NM_001348731.1:c.4551A>T	NP_001335660.1:p.Pro1517=
NM_001348732.1:c.4548A>T	NP_001335661.1:p.Pro1516=
NM_001348734.1:c.4437A>T	NP_001335663.1:p.Pro1479=
NM_001348735.1:c.4434A>T	NP_001335664.1:p.Pro1478=
NM_001348736.1:c.4308A>T	NP_001335665.1:p.Pro1436=
NM_001348738.1:c.3996+2013A>T	NP_001335667.1:n.3996+2013A>T
NM_001348739.1:c.3885+2013A>T	NP_001335668.1:n.3885+2013A>T
NM_001348740.1:c.3885+2013A>T	NP_001335669.1:n.3885+2013A>T
NM_001348741.1:c.3882+2013A>T	NP_001335670.1:n.3882+2013A>T
NM_001348742.1:c.3882+2013A>T	NP_001335671.1:n.3882+2013A>T
NM_001348743.1:c.3882+2013A>T	NP_001335672.1:n.3882+2013A>T
NM_020738.3:c.4605A>T	NP_065789.1:p.Pro1535=
NR_145964.1:n.4252+2013A>T
NR_145965.1:n.4078+2013A>T
NM_001348729.2:c.4608A>T	NP_001335658.1:p.Pro1536=
NM_001348731.2:c.4551A>T	NP_001335660.1:p.Pro1517=
NM_001348732.2:c.4548A>T	NP_001335661.1:p.Pro1516=
NM_001348734.2:c.4437A>T	NP_001335663.1:p.Pro1479=
NM_001348735.2:c.4434A>T	NP_001335664.1:p.Pro1478=
NM_001348736.2:c.4308A>T	NP_001335665.1:p.Pro1436=
NM_001348738.2:c.3996+2013A>T	NP_001335667.1:n.3996+2013A>T
NM_001348739.2:c.3885+2013A>T	NP_001335668.1:n.3885+2013A>T
NM_001348740.2:c.3885+2013A>T	NP_001335669.1:n.3885+2013A>T
NM_001348741.2:c.3882+2013A>T	NP_001335670.1:n.3882+2013A>T
NM_001348742.2:c.3882+2013A>T	NP_001335671.1:n.3882+2013A>T
NM_001348743.2:c.3882+2013A>T	NP_001335672.1:n.3882+2013A>T
NM_020738.4:c.4605A>T MANE Select	NP_065789.1:p.Pro1535=
NR_145964.2:n.4226+2013A>T
NR_145965.2:n.4052+2013A>T