Canonical Allele Identifier: CA6677549
Community Standard Title: NM_020401.4(NUP107):c.790C>T (p.Arg264Ter)
Gene: NUP107 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000012.12:g.68709298C>T , CM000674.2:g.68709298C>T GRCh38
NC_000012.11:g.69103078C>T , CM000674.1:g.69103078C>T GRCh37
NC_000012.10:g.67389345C>T NCBI36
NG_046600.2:g.27348C>T

Transcript Alleles

HGVS Amino-acid Change
NM_020401.4:c.790C>T MANE Select NP_065134.1:p.Arg264Ter
ENST00000229179.9:c.790C>T MANE Select ENSP00000229179.4:p.Arg264Ter
NM_001330192.1:c.703C>T NP_001317121.1:p.Arg235Ter
NM_001330192.2:c.703C>T NP_001317121.1:p.Arg235Ter
NM_020401.2:c.790C>T NP_065134.1:p.Arg264Ter
NM_020401.3:c.790C>T NP_065134.1:p.Arg264Ter
ENST00000229179.8:c.790C>T ENSP00000229179.4:p.Arg264Ter
ENST00000378905.6:c.337C>T ENSP00000368185.2:p.Arg113Ter
ENST00000535718.5:c.*333C>T ENSP00000445567.1:n.*333C>T
ENST00000537662.1:n.76C>T
ENST00000539906.5:c.703C>T ENSP00000441448.1:p.Arg235Ter
XM_005269037.2:c.790C>T XP_005269094.1:p.Arg264Ter
XM_005269037.4:c.790C>T XP_005269094.1:p.Arg264Ter
XM_011538576.1:c.703C>T XP_011536878.1:p.Arg235Ter