Canonical Allele Identifier: CA5424762
Gene: CUBN HGNC NCBI

Linked Data

ClinVar Variation Id: 860120
ClinVar RCV Id: RCV001066372
dbSNP Id: rs778092585
ExAC: 10:17107545 C / G
gnomAD v2: 10-17107545-C-G
gnomAD v3: 10-17065546-C-G
gnomAD v4: 10-17065546-C-G
MyVariant Identifiers: chr10:g.17107545C>G (hg19) chr10:g.17065546C>G (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17065546C>G , CM000672.2:g.17065546C>G GRCh38
NC_000010.10:g.17107545C>G , CM000672.1:g.17107545C>G GRCh37
NC_000010.9:g.17147551C>G NCBI36
NG_008967.1:g.69272G>C , LRG_540:g.69272G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.3101G>C MANE Select ENSP00000367064.4:p.Gly1034Ala
ENST00000377833.8:c.3101G>C ENSP00000367064.4:p.Gly1034Ala
NM_001081.3:c.3101G>C , LRG_540t1:c.3101G>C NP_001072.2:p.Gly1034Ala
XM_011519708.1:c.3101G>C XP_011518010.1:p.Gly1034Ala
XM_011519708.2:c.3101G>C XP_011518010.1:p.Gly1034Ala
NM_001081.4:c.3101G>C MANE Select NP_001072.2:p.Gly1034Ala
Search 100 bp 5'
Search 100 bp 3'