Canonical Allele Identifier: CA5422614

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16840997A>G , CM000672.2:g.16840997A>G	GRCh38
NC_000010.10:g.16882996A>G , CM000672.1:g.16882996A>G	GRCh37
NC_000010.9:g.16923002A>G	NCBI36
NG_008967.1:g.293821T>C , LRG_540:g.293821T>C

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.9714T>C MANE Select	NP_001072.2:p.Gly3238=
ENST00000377833.10:c.9714T>C MANE Select	ENSP00000367064.4:p.Gly3238=
NM_001081.3:c.9714T>C , LRG_540t1:c.9714T>C	NP_001072.2:p.Gly3238=
ENST00000377833.8:c.9714T>C	ENSP00000367064.4:p.Gly3238=
ENST00000649135.1:n.309T>C
XM_011519709.1:c.5700T>C	XP_011518011.1:p.Gly1900=
XM_011519709.2:c.5700T>C	XP_011518011.1:p.Gly1900=
XM_011519710.1:c.5676T>C	XP_011518012.1:p.Gly1892=
XM_011519710.2:c.5676T>C	XP_011518012.1:p.Gly1892=
XM_011519711.1:c.5556T>C	XP_011518013.1:p.Gly1852=
XM_011519711.3:c.5556T>C	XP_011518013.1:p.Gly1852=