Canonical Allele Identifier: CA376123649

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16840413G>A , CM000672.2:g.16840413G>A	GRCh38
NC_000010.10:g.16882412G>A , CM000672.1:g.16882412G>A	GRCh37
NC_000010.9:g.16922418G>A	NCBI36
NG_008967.1:g.294405C>T , LRG_540:g.294405C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.9949C>T MANE Select	NP_001072.2:p.Gln3317Ter
ENST00000377833.10:c.9949C>T MANE Select	ENSP00000367064.4:p.Gln3317Ter
NM_001081.3:c.9949C>T , LRG_540t1:c.9949C>T	NP_001072.2:p.Gln3317Ter
ENST00000377833.8:c.9949C>T	ENSP00000367064.4:p.Gln3317Ter
ENST00000649135.1:n.544C>T
XM_011519709.1:c.5935C>T	XP_011518011.1:p.Gln1979Ter
XM_011519709.2:c.5935C>T	XP_011518011.1:p.Gln1979Ter
XM_011519710.1:c.5911C>T	XP_011518012.1:p.Gln1971Ter
XM_011519710.2:c.5911C>T	XP_011518012.1:p.Gln1971Ter
XM_011519711.1:c.5791C>T	XP_011518013.1:p.Gln1931Ter
XM_011519711.3:c.5791C>T	XP_011518013.1:p.Gln1931Ter