Canonical Allele Identifier: CA5425812
Gene: CUBN HGNC NCBI

Linked Data

dbSNP Id: rs770907287
ExAC: 10:17171744 A / T
gnomAD v2: 10-17171744-A-T
gnomAD v3: 10-17129745-A-T
gnomAD v4: 10-17129745-A-T
MyVariant Identifiers: chr10:g.17171744A>T (hg19) chr10:g.17129745A>T (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17129745A>T , CM000672.2:g.17129745A>T GRCh38
NC_000010.10:g.17171744A>T , CM000672.1:g.17171744A>T GRCh37
NC_000010.9:g.17211750A>T NCBI36
NG_008967.1:g.5073T>A , LRG_540:g.5073T>A

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.21T>A MANE Select ENSP00000367064.4:p.Pro7=
ENST00000377823.1:c.21T>A ENSP00000367054.1:p.Pro7=
ENST00000377833.8:c.21T>A ENSP00000367064.4:p.Pro7=
NM_001081.3:c.21T>A , LRG_540t1:c.21T>A NP_001072.2:p.Pro7=
XM_011519708.1:c.21T>A XP_011518010.1:p.Pro7=
XM_011519708.2:c.21T>A XP_011518010.1:p.Pro7=
NM_001081.4:c.21T>A MANE Select NP_001072.2:p.Pro7=
Search 100 bp 5'
Search 100 bp 3'