Canonical Allele Identifier: CA468299089

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16835083G>A , CM000672.2:g.16835083G>A	GRCh38
NC_000010.10:g.16877082G>A , CM000672.1:g.16877082G>A	GRCh37
NC_000010.9:g.16917088G>A	NCBI36
NG_008967.1:g.299735C>T , LRG_540:g.299735C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.10293C>T MANE Select	NP_001072.2:p.His3431=
ENST00000377833.10:c.10293C>T MANE Select	ENSP00000367064.4:p.His3431=
NM_001081.3:c.10293C>T , LRG_540t1:c.10293C>T	NP_001072.2:p.His3431=
ENST00000377833.8:c.10293C>T	ENSP00000367064.4:p.His3431=
XM_011519709.1:c.6279C>T	XP_011518011.1:p.His2093=
XM_011519709.2:c.6279C>T	XP_011518011.1:p.His2093=
XM_011519710.1:c.6255C>T	XP_011518012.1:p.His2085=
XM_011519710.2:c.6255C>T	XP_011518012.1:p.His2085=
XM_011519711.1:c.6135C>T	XP_011518013.1:p.His2045=
XM_011519711.3:c.6135C>T	XP_011518013.1:p.His2045=