Canonical Allele Identifier: CA376118634

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16867008C>A (hg19) ; chr10:g.16825009C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16825009C>A , CM000672.2:g.16825009C>A	GRCh38
NC_000010.10:g.16867008C>A , CM000672.1:g.16867008C>A	GRCh37
NC_000010.9:g.16907014C>A	NCBI36
NG_008967.1:g.309809G>T , LRG_540:g.309809G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.10838G>T MANE Select	ENSP00000367064.4:p.Arg3613Leu
ENST00000377833.8:c.10838G>T	ENSP00000367064.4:p.Arg3613Leu
NM_001081.3:c.10838G>T , LRG_540t1:c.10838G>T	NP_001072.2:p.Arg3613Leu
XM_011519709.1:c.6824G>T	XP_011518011.1:p.Arg2275Leu
XM_011519710.1:c.6800G>T	XP_011518012.1:p.Arg2267Leu
XM_011519711.1:c.6680G>T	XP_011518013.1:p.Arg2227Leu
XM_011519709.2:c.6824G>T	XP_011518011.1:p.Arg2275Leu
XM_011519710.2:c.6800G>T	XP_011518012.1:p.Arg2267Leu
XM_011519711.3:c.6680G>T	XP_011518013.1:p.Arg2227Leu
NM_001081.4:c.10838G>T MANE Select	NP_001072.2:p.Arg3613Leu