Canonical Allele Identifier: CA376121234

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16835131G>T , CM000672.2:g.16835131G>T	GRCh38
NC_000010.10:g.16877130G>T , CM000672.1:g.16877130G>T	GRCh37
NC_000010.9:g.16917136G>T	NCBI36
NG_008967.1:g.299687C>A , LRG_540:g.299687C>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.10245C>A MANE Select	NP_001072.2:p.Tyr3415Ter
ENST00000377833.10:c.10245C>A MANE Select	ENSP00000367064.4:p.Tyr3415Ter
NM_001081.3:c.10245C>A , LRG_540t1:c.10245C>A	NP_001072.2:p.Tyr3415Ter
ENST00000377833.8:c.10245C>A	ENSP00000367064.4:p.Tyr3415Ter
XM_011519709.1:c.6231C>A	XP_011518011.1:p.Tyr2077Ter
XM_011519709.2:c.6231C>A	XP_011518011.1:p.Tyr2077Ter
XM_011519710.1:c.6207C>A	XP_011518012.1:p.Tyr2069Ter
XM_011519710.2:c.6207C>A	XP_011518012.1:p.Tyr2069Ter
XM_011519711.1:c.6087C>A	XP_011518013.1:p.Tyr2029Ter
XM_011519711.3:c.6087C>A	XP_011518013.1:p.Tyr2029Ter