Canonical Allele Identifier: CA2574500106
Gene: CUBN HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16824927A>G , CM000672.2:g.16824927A>G GRCh38
NC_000010.10:g.16866926A>G , CM000672.1:g.16866926A>G GRCh37
NC_000010.9:g.16906932A>G NCBI36
NG_008967.1:g.309891T>C , LRG_540:g.309891T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.*48T>C MANE Select ENSP00000367064.4:n.*48T>C
ENST00000377833.8:c.*48T>C ENSP00000367064.4:n.*48T>C
NM_001081.3:c.*48T>C , LRG_540t1:c.*48T>C NP_001072.2:n.*48T>C
XM_011519709.1:c.*48T>C XP_011518011.1:n.*48T>C
XM_011519710.1:c.*48T>C XP_011518012.1:n.*48T>C
XM_011519711.1:c.*48T>C XP_011518013.1:n.*48T>C
XM_011519709.2:c.*48T>C XP_011518011.1:n.*48T>C
XM_011519710.2:c.*48T>C XP_011518012.1:n.*48T>C
XM_011519711.3:c.*48T>C XP_011518013.1:n.*48T>C
NM_001081.4:c.*48T>C MANE Select NP_001072.2:n.*48T>C
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