Canonical Allele Identifier: CA468307423
Gene: CUBN HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.17171744A>C (hg19)
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Genomic Alleles

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

Transcript Alleles

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