Canonical Allele Identifier: CA376158692
Gene: CUBN HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.17113438G>C (hg19) chr10:g.17071439G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17071439G>C , CM000672.2:g.17071439G>C GRCh38
NC_000010.10:g.17113438G>C , CM000672.1:g.17113438G>C GRCh37
NC_000010.9:g.17153444G>C NCBI36
NG_008967.1:g.63379C>G , LRG_540:g.63379C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.2612C>G MANE Select ENSP00000367064.4:p.Thr871Arg
ENST00000377833.8:c.2612C>G ENSP00000367064.4:p.Thr871Arg
NM_001081.3:c.2612C>G , LRG_540t1:c.2612C>G NP_001072.2:p.Thr871Arg
XM_011519708.1:c.2612C>G XP_011518010.1:p.Thr871Arg
XM_011519708.2:c.2612C>G XP_011518010.1:p.Thr871Arg
NM_001081.4:c.2612C>G MANE Select NP_001072.2:p.Thr871Arg
Search 100 bp 5'
Search 100 bp 3'