Canonical Allele Identifier: CA376119778

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16870821C>A (hg19) ; chr10:g.16828822C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16828822C>A , CM000672.2:g.16828822C>A	GRCh38
NC_000010.10:g.16870821C>A , CM000672.1:g.16870821C>A	GRCh37
NC_000010.9:g.16910827C>A	NCBI36
NG_008967.1:g.305996G>T , LRG_540:g.305996G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.10747G>T MANE Select	ENSP00000367064.4:p.Gly3583Ter
ENST00000377833.8:c.10747G>T	ENSP00000367064.4:p.Gly3583Ter
NM_001081.3:c.10747G>T , LRG_540t1:c.10747G>T	NP_001072.2:p.Gly3583Ter
XM_011519709.1:c.6733G>T	XP_011518011.1:p.Gly2245Ter
XM_011519710.1:c.6709G>T	XP_011518012.1:p.Gly2237Ter
XM_011519711.1:c.6589G>T	XP_011518013.1:p.Gly2197Ter
XM_011519709.2:c.6733G>T	XP_011518011.1:p.Gly2245Ter
XM_011519710.2:c.6709G>T	XP_011518012.1:p.Gly2237Ter
XM_011519711.3:c.6589G>T	XP_011518013.1:p.Gly2197Ter
NM_001081.4:c.10747G>T MANE Select	NP_001072.2:p.Gly3583Ter