Canonical Allele Identifier: CA376145019

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16984280C>G , CM000672.2:g.16984280C>G	GRCh38
NC_000010.10:g.17026279C>G , CM000672.1:g.17026279C>G	GRCh37
NC_000010.9:g.17066285C>G	NCBI36
NG_008967.1:g.150538G>C , LRG_540:g.150538G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.4351-1G>C MANE Select	NP_001072.2:n.4351-1G>C
ENST00000377833.10:c.4351-1G>C MANE Select	ENSP00000367064.4:n.4351-1G>C
NM_001081.3:c.4351-1G>C , LRG_540t1:c.4351-1G>C	NP_001072.2:n.4351-1G>C
ENST00000377833.8:c.4351-1G>C	ENSP00000367064.4:n.4351-1G>C
XM_011519708.1:c.4351-1G>C	XP_011518010.1:n.4351-1G>C
XM_011519708.2:c.4351-1G>C	XP_011518010.1:n.4351-1G>C
XM_011519709.1:c.337-1G>C	XP_011518011.1:n.337-1G>C
XM_011519709.2:c.337-1G>C	XP_011518011.1:n.337-1G>C
XM_011519710.1:c.313-1G>C	XP_011518012.1:n.313-1G>C
XM_011519710.2:c.313-1G>C	XP_011518012.1:n.313-1G>C
XM_011519711.1:c.193-1G>C	XP_011518013.1:n.193-1G>C
XM_011519711.3:c.193-1G>C	XP_011518013.1:n.193-1G>C