Canonical Allele Identifier: CA468307204
Gene: CUBN HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.17168760C>T (hg19)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17126761C>T , CM000672.2:g.17126761C>T GRCh38
NC_000010.10:g.17168760C>T , CM000672.1:g.17168760C>T GRCh37
NC_000010.9:g.17208766C>T NCBI36
NG_008967.1:g.8057G>A , LRG_540:g.8057G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.387G>A MANE Select ENSP00000367064.4:p.Gln129=
ENST00000377823.1:c.387G>A ENSP00000367054.1:p.Gln129=
ENST00000377833.8:c.387G>A ENSP00000367064.4:p.Gln129=
ENST00000433666.5:c.48G>A ENSP00000415970.1:p.Gln16=
NM_001081.3:c.387G>A , LRG_540t1:c.387G>A NP_001072.2:p.Gln129=
XM_011519708.1:c.387G>A XP_011518010.1:p.Gln129=
XM_011519708.2:c.387G>A XP_011518010.1:p.Gln129=
NM_001081.4:c.387G>A MANE Select NP_001072.2:p.Gln129=
Search 100 bp 5'
Search 100 bp 3'