Canonical Allele Identifier: CA2608405406
Gene: CUBN HGNC NCBI

Linked Data

gnomAD v4: 10-17129773-C-G
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17129773C>G , CM000672.2:g.17129773C>G GRCh38
NC_000010.10:g.17171772C>G , CM000672.1:g.17171772C>G GRCh37
NC_000010.9:g.17211778C>G NCBI36
NG_008967.1:g.5045G>C , LRG_540:g.5045G>C

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.-8G>C MANE Select ENSP00000367064.4:n.-8G>C
ENST00000377823.1:c.-8G>C ENSP00000367054.1:n.-8G>C
ENST00000377833.8:c.-8G>C ENSP00000367064.4:n.-8G>C
NM_001081.3:c.-8G>C , LRG_540t1:c.-8G>C NP_001072.2:n.-8G>C
XM_011519708.1:c.-8G>C XP_011518010.1:n.-8G>C
XM_011519708.2:c.-8G>C XP_011518010.1:n.-8G>C
NM_001081.4:c.-8G>C MANE Select NP_001072.2:n.-8G>C
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