Canonical Allele Identifier: CA468298486

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16867010C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16825011C>A , CM000672.2:g.16825011C>A	GRCh38
NC_000010.10:g.16867010C>A , CM000672.1:g.16867010C>A	GRCh37
NC_000010.9:g.16907016C>A	NCBI36
NG_008967.1:g.309807G>T , LRG_540:g.309807G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.10836G>T MANE Select	ENSP00000367064.4:p.Arg3612=
ENST00000377833.8:c.10836G>T	ENSP00000367064.4:p.Arg3612=
NM_001081.3:c.10836G>T , LRG_540t1:c.10836G>T	NP_001072.2:p.Arg3612=
XM_011519709.1:c.6822G>T	XP_011518011.1:p.Arg2274=
XM_011519710.1:c.6798G>T	XP_011518012.1:p.Arg2266=
XM_011519711.1:c.6678G>T	XP_011518013.1:p.Arg2226=
XM_011519709.2:c.6822G>T	XP_011518011.1:p.Arg2274=
XM_011519710.2:c.6798G>T	XP_011518012.1:p.Arg2266=
XM_011519711.3:c.6678G>T	XP_011518013.1:p.Arg2226=
NM_001081.4:c.10836G>T MANE Select	NP_001072.2:p.Arg3612=