Canonical Allele Identifier: CA813186189
Gene: NSUN2 HGNC NCBI

Linked Data

dbSNP Id: rs1265894830
MyVariant Identifiers: chr5:g.6620059del (hg19) chr5:g.6619946del (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000005.10:g.6619946del , CM000667.2:g.6619946del GRCh38
NC_000005.9:g.6620059del , CM000667.1:g.6620059del GRCh37
NC_000005.8:g.6673059del NCBI36
NG_028215.1:g.18415del

Transcript Alleles

HGVS Amino-acid Change
ENST00000264670.11:c.815+160del MANE Select ENSP00000264670.6:n.815+160del
ENST00000264670.10:c.815+160del ENSP00000264670.6:n.815+160del
ENST00000504374.5:c.*121+160del ENSP00000421783.1:n.*121+160del
ENST00000505892.5:n.1384+160del
ENST00000506139.5:c.710+160del ENSP00000420957.1:n.710+160del
NM_001193455.1:c.710+160del NP_001180384.1:n.710+160del
NM_017755.5:c.815+160del NP_060225.4:n.815+160del
NR_037947.1:n.1111+160del
NM_017755.6:c.815+160del MANE Select NP_060225.4:n.815+160del
NM_001193455.2:c.710+160del NP_001180384.1:n.710+160del
NR_037947.2:n.795+160del
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