Canonical Allele Identifier: CA2608396425
Gene: CUBN HGNC NCBI

Linked Data

gnomAD v4: 10-16828735-A-G
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16828735A>G , CM000672.2:g.16828735A>G GRCh38
NC_000010.10:g.16870734A>G , CM000672.1:g.16870734A>G GRCh37
NC_000010.9:g.16910740A>G NCBI36
NG_008967.1:g.306083T>C , LRG_540:g.306083T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.10764+70T>C MANE Select ENSP00000367064.4:n.10764+70T>C
ENST00000377833.8:c.10764+70T>C ENSP00000367064.4:n.10764+70T>C
NM_001081.3:c.10764+70T>C , LRG_540t1:c.10764+70T>C NP_001072.2:n.10764+70T>C
XM_011519709.1:c.6750+70T>C XP_011518011.1:n.6750+70T>C
XM_011519710.1:c.6726+70T>C XP_011518012.1:n.6726+70T>C
XM_011519711.1:c.6606+70T>C XP_011518013.1:n.6606+70T>C
XM_011519709.2:c.6750+70T>C XP_011518011.1:n.6750+70T>C
XM_011519710.2:c.6726+70T>C XP_011518012.1:n.6726+70T>C
XM_011519711.3:c.6606+70T>C XP_011518013.1:n.6606+70T>C
NM_001081.4:c.10764+70T>C MANE Select NP_001072.2:n.10764+70T>C
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