Canonical Allele Identifier: CA5423257

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16906391G>C , CM000672.2:g.16906391G>C	GRCh38
NC_000010.10:g.16948390G>C , CM000672.1:g.16948390G>C	GRCh37
NC_000010.9:g.16988396G>C	NCBI36
NG_008967.1:g.228427C>G , LRG_540:g.228427C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7724C>G MANE Select	ENSP00000367064.4:p.Pro2575Arg
ENST00000648092.1:n.260C>G
ENST00000649933.1:n.86C>G
ENST00000377833.8:c.7724C>G	ENSP00000367064.4:p.Pro2575Arg
NM_001081.3:c.7724C>G , LRG_540t1:c.7724C>G	NP_001072.2:p.Pro2575Arg
XM_011519708.1:c.7724C>G	XP_011518010.1:p.Pro2575Arg
XM_011519709.1:c.3710C>G	XP_011518011.1:p.Pro1237Arg
XM_011519710.1:c.3686C>G	XP_011518012.1:p.Pro1229Arg
XM_011519711.1:c.3566C>G	XP_011518013.1:p.Pro1189Arg
XM_011519708.2:c.7724C>G	XP_011518010.1:p.Pro2575Arg
XM_011519709.2:c.3710C>G	XP_011518011.1:p.Pro1237Arg
XM_011519710.2:c.3686C>G	XP_011518012.1:p.Pro1229Arg
XM_011519711.3:c.3566C>G	XP_011518013.1:p.Pro1189Arg
NM_001081.4:c.7724C>G MANE Select	NP_001072.2:p.Pro2575Arg