Canonical Allele Identifier: CA5423703

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16925687C>T , CM000672.2:g.16925687C>T	GRCh38
NC_000010.10:g.16967686C>T , CM000672.1:g.16967686C>T	GRCh37
NC_000010.9:g.17007692C>T	NCBI36
NG_008967.1:g.209131G>A , LRG_540:g.209131G>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.6359G>A MANE Select	ENSP00000367064.4:p.Trp2120Ter
ENST00000377833.8:c.6359G>A	ENSP00000367064.4:p.Trp2120Ter
NM_001081.3:c.6359G>A , LRG_540t1:c.6359G>A	NP_001072.2:p.Trp2120Ter
XM_011519708.1:c.6359G>A	XP_011518010.1:p.Trp2120Ter
XM_011519709.1:c.2345G>A	XP_011518011.1:p.Trp782Ter
XM_011519710.1:c.2321G>A	XP_011518012.1:p.Trp774Ter
XM_011519711.1:c.2201G>A	XP_011518013.1:p.Trp734Ter
XM_011519708.2:c.6359G>A	XP_011518010.1:p.Trp2120Ter
XM_011519709.2:c.2345G>A	XP_011518011.1:p.Trp782Ter
XM_011519710.2:c.2321G>A	XP_011518012.1:p.Trp774Ter
XM_011519711.3:c.2201G>A	XP_011518013.1:p.Trp734Ter
NM_001081.4:c.6359G>A MANE Select	NP_001072.2:p.Trp2120Ter