Canonical Allele Identifier: CA376118516

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16866978C>A (hg19) ; chr10:g.16824979C>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16824979C>A , CM000672.2:g.16824979C>A	GRCh38
NC_000010.10:g.16866978C>A , CM000672.1:g.16866978C>A	GRCh37
NC_000010.9:g.16906984C>A	NCBI36
NG_008967.1:g.309839G>T , LRG_540:g.309839G>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.10868G>T MANE Select	ENSP00000367064.4:p.Ser3623Ile
ENST00000377833.8:c.10868G>T	ENSP00000367064.4:p.Ser3623Ile
NM_001081.3:c.10868G>T , LRG_540t1:c.10868G>T	NP_001072.2:p.Ser3623Ile
XM_011519709.1:c.6854G>T	XP_011518011.1:p.Ser2285Ile
XM_011519710.1:c.6830G>T	XP_011518012.1:p.Ser2277Ile
XM_011519711.1:c.6710G>T	XP_011518013.1:p.Ser2237Ile
XM_011519709.2:c.6854G>T	XP_011518011.1:p.Ser2285Ile
XM_011519710.2:c.6830G>T	XP_011518012.1:p.Ser2277Ile
XM_011519711.3:c.6710G>T	XP_011518013.1:p.Ser2237Ile
NM_001081.4:c.10868G>T MANE Select	NP_001072.2:p.Ser3623Ile