Canonical Allele Identifier: CA662380968
Gene: CUBN HGNC NCBI

Linked Data

dbSNP Id: rs1270578921
gnomAD v3: 10-17129771-T-A
gnomAD v4: 10-17129771-T-A
MyVariant Identifiers: chr10:g.17171770T>A (hg19) chr10:g.17129771T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17129771T>A , CM000672.2:g.17129771T>A GRCh38
NC_000010.10:g.17171770T>A , CM000672.1:g.17171770T>A GRCh37
NC_000010.9:g.17211776T>A NCBI36
NG_008967.1:g.5047A>T , LRG_540:g.5047A>T

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.-6A>T MANE Select ENSP00000367064.4:n.-6A>T
ENST00000377823.1:c.-6A>T ENSP00000367054.1:n.-6A>T
ENST00000377833.8:c.-6A>T ENSP00000367064.4:n.-6A>T
NM_001081.3:c.-6A>T , LRG_540t1:c.-6A>T NP_001072.2:n.-6A>T
XM_011519708.1:c.-6A>T XP_011518010.1:n.-6A>T
XM_011519708.2:c.-6A>T XP_011518010.1:n.-6A>T
NM_001081.4:c.-6A>T MANE Select NP_001072.2:n.-6A>T
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