Canonical Allele Identifier: CA5422347

Gene: CUBN

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16828994G>A , CM000672.2:g.16828994G>A	GRCh38
NC_000010.10:g.16870993G>A , CM000672.1:g.16870993G>A	GRCh37
NC_000010.9:g.16910999G>A	NCBI36
NG_008967.1:g.305824C>T , LRG_540:g.305824C>T

Transcript Alleles

HGVS	Amino-acid Change
NM_001081.4:c.10575C>T MANE Select	NP_001072.2:p.Pro3525=
ENST00000377833.10:c.10575C>T MANE Select	ENSP00000367064.4:p.Pro3525=
NM_001081.3:c.10575C>T , LRG_540t1:c.10575C>T	NP_001072.2:p.Pro3525=
ENST00000377833.8:c.10575C>T	ENSP00000367064.4:p.Pro3525=
XM_011519709.1:c.6561C>T	XP_011518011.1:p.Pro2187=
XM_011519709.2:c.6561C>T	XP_011518011.1:p.Pro2187=
XM_011519710.1:c.6537C>T	XP_011518012.1:p.Pro2179=
XM_011519710.2:c.6537C>T	XP_011518012.1:p.Pro2179=
XM_011519711.1:c.6417C>T	XP_011518013.1:p.Pro2139=
XM_011519711.3:c.6417C>T	XP_011518013.1:p.Pro2139=