Canonical Allele Identifier: CA468307289
Gene: CUBN HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.17171126T>C (hg19)

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17129127T>C , CM000672.2:g.17129127T>C GRCh38
NC_000010.10:g.17171126T>C , CM000672.1:g.17171126T>C GRCh37
NC_000010.9:g.17211132T>C NCBI36
NG_008967.1:g.5691A>G , LRG_540:g.5691A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.246A>G MANE Select ENSP00000367064.4:p.Leu82=
ENST00000377823.1:c.246A>G ENSP00000367054.1:p.Leu82=
ENST00000377833.8:c.246A>G ENSP00000367064.4:p.Leu82=
NM_001081.3:c.246A>G , LRG_540t1:c.246A>G NP_001072.2:p.Leu82=
XM_011519708.1:c.246A>G XP_011518010.1:p.Leu82=
XM_011519708.2:c.246A>G XP_011518010.1:p.Leu82=
NM_001081.4:c.246A>G MANE Select NP_001072.2:p.Leu82=