Canonical Allele Identifier: CA376169598
Gene: CUBN HGNC NCBI

Linked Data

MyVariant Identifiers: chr10:g.17171124T>A (hg19) chr10:g.17129125T>A (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.17129125T>A , CM000672.2:g.17129125T>A GRCh38
NC_000010.10:g.17171124T>A , CM000672.1:g.17171124T>A GRCh37
NC_000010.9:g.17211130T>A NCBI36
NG_008967.1:g.5693A>T , LRG_540:g.5693A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.248A>T MANE Select ENSP00000367064.4:p.His83Leu
ENST00000377823.1:c.248A>T ENSP00000367054.1:p.His83Leu
ENST00000377833.8:c.248A>T ENSP00000367064.4:p.His83Leu
NM_001081.3:c.248A>T , LRG_540t1:c.248A>T NP_001072.2:p.His83Leu
XM_011519708.1:c.248A>T XP_011518010.1:p.His83Leu
XM_011519708.2:c.248A>T XP_011518010.1:p.His83Leu
NM_001081.4:c.248A>T MANE Select NP_001072.2:p.His83Leu
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