Canonical Allele Identifier: CA376127062

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16869655C>G , CM000672.2:g.16869655C>G	GRCh38
NC_000010.10:g.16911654C>G , CM000672.1:g.16911654C>G	GRCh37
NC_000010.9:g.16951660C>G	NCBI36
NG_008967.1:g.265163G>C , LRG_540:g.265163G>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.9435G>C MANE Select	NP_001072.2:p.Met3145Ile
ENST00000377833.10:c.9435G>C MANE Select	ENSP00000367064.4:p.Met3145Ile
NM_001081.3:c.9435G>C , LRG_540t1:c.9435G>C	NP_001072.2:p.Met3145Ile
ENST00000377833.8:c.9435G>C	ENSP00000367064.4:p.Met3145Ile
XM_011519709.1:c.5421G>C	XP_011518011.1:p.Met1807Ile
XM_011519709.2:c.5421G>C	XP_011518011.1:p.Met1807Ile
XM_011519710.1:c.5397G>C	XP_011518012.1:p.Met1799Ile
XM_011519710.2:c.5397G>C	XP_011518012.1:p.Met1799Ile
XM_011519711.1:c.5277G>C	XP_011518013.1:p.Met1759Ile
XM_011519711.3:c.5277G>C	XP_011518013.1:p.Met1759Ile