Canonical Allele Identifier: CA345764058

Gene: KIDINS220

Linked Data

• MyVariant Identifiers: chr2:g.8871658A>G (hg19) ; chr2:g.8731528A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000002.12:g.8731528A>G , CM000664.2:g.8731528A>G	GRCh38
NC_000002.11:g.8871658A>G , CM000664.1:g.8871658A>G	GRCh37
NC_000002.10:g.8789109A>G	NCBI36
NG_053168.1:g.111112T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000685097.1:c.4211T>C	ENSP00000510510.1:p.Phe1404Ser
ENST00000686383.1:n.4393T>C
ENST00000686906.1:c.*396T>C	ENSP00000508907.1:n.*396T>C
ENST00000687894.1:c.*1880T>C	ENSP00000509577.1:n.*1880T>C
ENST00000687912.1:c.4013T>C	ENSP00000508455.1:p.Phe1338Ser
ENST00000689369.1:c.3882+1916T>C	ENSP00000509856.1:n.3882+1916T>C
ENST00000689852.1:c.3915+1916T>C	ENSP00000510537.1:n.3915+1916T>C
ENST00000691030.1:c.4487T>C	ENSP00000510148.1:p.Phe1496Ser
ENST00000693394.1:c.3882+1916T>C	ENSP00000509014.1:n.3882+1916T>C
ENST00000693432.1:c.4053+1916T>C	ENSP00000510486.1:n.4053+1916T>C
ENST00000693597.1:n.861+1916T>C
ENST00000256707.8:c.4508T>C MANE Select	ENSP00000256707.4:p.Phe1503Ser
ENST00000569008.2:c.3882+1916T>C	ENSP00000491461.1:n.3882+1916T>C
ENST00000256707.7:c.4508T>C	ENSP00000256707.3:p.Phe1503Ser
ENST00000473731.5:c.4451T>C	ENSP00000418974.1:p.Phe1484Ser
ENST00000488729.5:c.*4397T>C	ENSP00000417390.1:n.*4397T>C
ENST00000496383.5:c.3123+1916T>C	ENSP00000420364.1:n.3123+1916T>C
NM_020738.2:c.4508T>C	NP_065789.1:p.Phe1503Ser
NM_001348729.1:c.4511T>C	NP_001335658.1:p.Phe1504Ser
NM_001348731.1:c.4454T>C	NP_001335660.1:p.Phe1485Ser
NM_001348732.1:c.4451T>C	NP_001335661.1:p.Phe1484Ser
NM_001348734.1:c.4340T>C	NP_001335663.1:p.Phe1447Ser
NM_001348735.1:c.4337T>C	NP_001335664.1:p.Phe1446Ser
NM_001348736.1:c.4211T>C	NP_001335665.1:p.Phe1404Ser
NM_001348738.1:c.3996+1916T>C	NP_001335667.1:n.3996+1916T>C
NM_001348739.1:c.3885+1916T>C	NP_001335668.1:n.3885+1916T>C
NM_001348740.1:c.3885+1916T>C	NP_001335669.1:n.3885+1916T>C
NM_001348741.1:c.3882+1916T>C	NP_001335670.1:n.3882+1916T>C
NM_001348742.1:c.3882+1916T>C	NP_001335671.1:n.3882+1916T>C
NM_001348743.1:c.3882+1916T>C	NP_001335672.1:n.3882+1916T>C
NM_020738.3:c.4508T>C	NP_065789.1:p.Phe1503Ser
NR_145964.1:n.4252+1916T>C
NR_145965.1:n.4078+1916T>C
NM_001348729.2:c.4511T>C	NP_001335658.1:p.Phe1504Ser
NM_001348731.2:c.4454T>C	NP_001335660.1:p.Phe1485Ser
NM_001348732.2:c.4451T>C	NP_001335661.1:p.Phe1484Ser
NM_001348734.2:c.4340T>C	NP_001335663.1:p.Phe1447Ser
NM_001348735.2:c.4337T>C	NP_001335664.1:p.Phe1446Ser
NM_001348736.2:c.4211T>C	NP_001335665.1:p.Phe1404Ser
NM_001348738.2:c.3996+1916T>C	NP_001335667.1:n.3996+1916T>C
NM_001348739.2:c.3885+1916T>C	NP_001335668.1:n.3885+1916T>C
NM_001348740.2:c.3885+1916T>C	NP_001335669.1:n.3885+1916T>C
NM_001348741.2:c.3882+1916T>C	NP_001335670.1:n.3882+1916T>C
NM_001348742.2:c.3882+1916T>C	NP_001335671.1:n.3882+1916T>C
NM_001348743.2:c.3882+1916T>C	NP_001335672.1:n.3882+1916T>C
NM_020738.4:c.4508T>C MANE Select	NP_065789.1:p.Phe1503Ser
NR_145964.2:n.4226+1916T>C
NR_145965.2:n.4052+1916T>C