Canonical Allele Identifier: CA5422276

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16825012C>T , CM000672.2:g.16825012C>T	GRCh38
NC_000010.10:g.16867011C>T , CM000672.1:g.16867011C>T	GRCh37
NC_000010.9:g.16907017C>T	NCBI36
NG_008967.1:g.309806G>A , LRG_540:g.309806G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.10835G>A MANE Select	NP_001072.2:p.Arg3612Gln
ENST00000377833.10:c.10835G>A MANE Select	ENSP00000367064.4:p.Arg3612Gln
NM_001081.3:c.10835G>A , LRG_540t1:c.10835G>A	NP_001072.2:p.Arg3612Gln
ENST00000377833.8:c.10835G>A	ENSP00000367064.4:p.Arg3612Gln
XM_011519709.1:c.6821G>A	XP_011518011.1:p.Arg2274Gln
XM_011519709.2:c.6821G>A	XP_011518011.1:p.Arg2274Gln
XM_011519710.1:c.6797G>A	XP_011518012.1:p.Arg2266Gln
XM_011519710.2:c.6797G>A	XP_011518012.1:p.Arg2266Gln
XM_011519711.1:c.6677G>A	XP_011518013.1:p.Arg2226Gln
XM_011519711.3:c.6677G>A	XP_011518013.1:p.Arg2226Gln