Canonical Allele Identifier: CA376143354

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16906313C>T , CM000672.2:g.16906313C>T	GRCh38
NC_000010.10:g.16948312C>T , CM000672.1:g.16948312C>T	GRCh37
NC_000010.9:g.16988318C>T	NCBI36
NG_008967.1:g.228505G>A , LRG_540:g.228505G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.7802G>A MANE Select	NP_001072.2:p.Trp2601Ter
ENST00000377833.10:c.7802G>A MANE Select	ENSP00000367064.4:p.Trp2601Ter
NM_001081.3:c.7802G>A , LRG_540t1:c.7802G>A	NP_001072.2:p.Trp2601Ter
ENST00000377833.8:c.7802G>A	ENSP00000367064.4:p.Trp2601Ter
ENST00000648092.1:n.338G>A
ENST00000649933.1:n.164G>A
XM_011519708.1:c.7802G>A	XP_011518010.1:p.Trp2601Ter
XM_011519708.2:c.7802G>A	XP_011518010.1:p.Trp2601Ter
XM_011519709.1:c.3788G>A	XP_011518011.1:p.Trp1263Ter
XM_011519709.2:c.3788G>A	XP_011518011.1:p.Trp1263Ter
XM_011519710.1:c.3764G>A	XP_011518012.1:p.Trp1255Ter
XM_011519710.2:c.3764G>A	XP_011518012.1:p.Trp1255Ter
XM_011519711.1:c.3644G>A	XP_011518013.1:p.Trp1215Ter
XM_011519711.3:c.3644G>A	XP_011518013.1:p.Trp1215Ter