Canonical Allele Identifier: CA1893313676
Gene: CUBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16828722T= , CM000672.2:g.16828722T= GRCh38
NC_000010.10:g.16870721T= , CM000672.1:g.16870721T= GRCh37
NC_000010.9:g.16910727T= NCBI36
NG_008967.1:g.306096A= , LRG_540:g.306096A=

Transcript Alleles

HGVS Amino-acid change
ENST00000377833.10:c.10764+83A= MANE Select ENSP00000367064.4:n.10764+83A=
ENST00000377833.8:c.10764+83A= ENSP00000367064.4:n.10764+83A=
NM_001081.3:c.10764+83A= , LRG_540t1:c.10764+83A= NP_001072.2:n.10764+83A=
XM_011519709.1:c.6750+83A= XP_011518011.1:n.6750+83A=
XM_011519710.1:c.6726+83A= XP_011518012.1:n.6726+83A=
XM_011519711.1:c.6606+83A= XP_011518013.1:n.6606+83A=
XM_011519709.2:c.6750+83A= XP_011518011.1:n.6750+83A=
XM_011519710.2:c.6726+83A= XP_011518012.1:n.6726+83A=
XM_011519711.3:c.6606+83A= XP_011518013.1:n.6606+83A=
NM_001081.4:c.10764+83A= MANE Select NP_001072.2:n.10764+83A=