Canonical Allele Identifier: CA5422934

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16890385G>A , CM000672.2:g.16890385G>A	GRCh38
NC_000010.10:g.16932384G>A , CM000672.1:g.16932384G>A	GRCh37
NC_000010.9:g.16972390G>A	NCBI36
NG_008967.1:g.244433C>T , LRG_540:g.244433C>T

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.8741C>T MANE Select	ENSP00000367064.4:p.Ala2914Val
ENST00000377833.8:c.8741C>T	ENSP00000367064.4:p.Ala2914Val
NM_001081.3:c.8741C>T , LRG_540t1:c.8741C>T	NP_001072.2:p.Ala2914Val
XM_011519709.1:c.4727C>T	XP_011518011.1:p.Ala1576Val
XM_011519710.1:c.4703C>T	XP_011518012.1:p.Ala1568Val
XM_011519711.1:c.4583C>T	XP_011518013.1:p.Ala1528Val
XM_011519709.2:c.4727C>T	XP_011518011.1:p.Ala1576Val
XM_011519710.2:c.4703C>T	XP_011518012.1:p.Ala1568Val
XM_011519711.3:c.4583C>T	XP_011518013.1:p.Ala1528Val
NM_001081.4:c.8741C>T MANE Select	NP_001072.2:p.Ala2914Val