Canonical Allele Identifier: CA203594978
Gene: CUBN HGNC NCBI
MyVariant.info:
GRCh38 chr10:g.17100527G>T
GRCh37 chr10:g.17142526G>T
gnomAD v2:
10:17142526 G / T
gnomAD v3:
10:17100527 G / T
gnomAD v4:
chr10-17100527-G-T
Joint Max Group AF 0.72287101 (NFE)
Genomes Max Group AF 0.72287101 (NFE)
ClinVar RCV:
RCV001649997
ClinVar Variation:
1249861
dbSNP:
6602175
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17100527G>T , CM000672.2:g.17100527G>T GRCh38
NC_000010.10:g.17142526G>T , CM000672.1:g.17142526G>T GRCh37
NC_000010.9:g.17182532G>T NCBI36
NG_008967.1:g.34291C>A , LRG_540:g.34291C>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.1531-288C>A MANE Select ENSP00000367064.4:n.1531-288C>A
ENST00000377833.8:c.1531-288C>A ENSP00000367064.4:n.1531-288C>A
NM_001081.3:c.1531-288C>A , LRG_540t1:c.1531-288C>A NP_001072.2:n.1531-288C>A
XM_011519708.1:c.1531-288C>A XP_011518010.1:n.1531-288C>A
XM_011519708.2:c.1531-288C>A XP_011518010.1:n.1531-288C>A
NM_001081.4:c.1531-288C>A MANE Select NP_001072.2:n.1531-288C>A
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