Canonical Allele Identifier: CA662288844
Gene: CUBN HGNC NCBI

Linked Data

dbSNP Id: rs1436843940
MyVariant Identifiers: chr10:g.16866780A>G (hg19) chr10:g.16824781A>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16824781A>G , CM000672.2:g.16824781A>G GRCh38
NC_000010.10:g.16866780A>G , CM000672.1:g.16866780A>G GRCh37
NC_000010.9:g.16906786A>G NCBI36
NG_008967.1:g.310037T>C , LRG_540:g.310037T>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.*194T>C MANE Select ENSP00000367064.4:n.*194T>C
ENST00000377833.8:c.*194T>C ENSP00000367064.4:n.*194T>C
NM_001081.3:c.*194T>C , LRG_540t1:c.*194T>C NP_001072.2:n.*194T>C
XM_011519709.1:c.*194T>C XP_011518011.1:n.*194T>C
XM_011519710.1:c.*194T>C XP_011518012.1:n.*194T>C
XM_011519711.1:c.*194T>C XP_011518013.1:n.*194T>C
XM_011519709.2:c.*194T>C XP_011518011.1:n.*194T>C
XM_011519710.2:c.*194T>C XP_011518012.1:n.*194T>C
XM_011519711.3:c.*194T>C XP_011518013.1:n.*194T>C
NM_001081.4:c.*194T>C MANE Select NP_001072.2:n.*194T>C
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