Canonical Allele Identifier: CA376121112

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16835082T>A , CM000672.2:g.16835082T>A	GRCh38
NC_000010.10:g.16877081T>A , CM000672.1:g.16877081T>A	GRCh37
NC_000010.9:g.16917087T>A	NCBI36
NG_008967.1:g.299736A>T , LRG_540:g.299736A>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.10294A>T MANE Select	ENSP00000367064.4:p.Thr3432Ser
ENST00000377833.8:c.10294A>T	ENSP00000367064.4:p.Thr3432Ser
NM_001081.3:c.10294A>T , LRG_540t1:c.10294A>T	NP_001072.2:p.Thr3432Ser
XM_011519709.1:c.6280A>T	XP_011518011.1:p.Thr2094Ser
XM_011519710.1:c.6256A>T	XP_011518012.1:p.Thr2086Ser
XM_011519711.1:c.6136A>T	XP_011518013.1:p.Thr2046Ser
XM_011519709.2:c.6280A>T	XP_011518011.1:p.Thr2094Ser
XM_011519710.2:c.6256A>T	XP_011518012.1:p.Thr2086Ser
XM_011519711.3:c.6136A>T	XP_011518013.1:p.Thr2046Ser
NM_001081.4:c.10294A>T MANE Select	NP_001072.2:p.Thr3432Ser