Canonical Allele Identifier: CA376155936
Community Standard Title: NM_001081.4(CUBN):c.5701G>T (p.Glu1901Ter)
Gene: CUBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16938995C>A , CM000672.2:g.16938995C>A GRCh38
NC_000010.10:g.16980994C>A , CM000672.1:g.16980994C>A GRCh37
NC_000010.9:g.17021000C>A NCBI36
NG_008967.1:g.195823G>T , LRG_540:g.195823G>T

Transcript Alleles

HGVS Amino-acid Change
NM_001081.4:c.5701G>T MANE Select NP_001072.2:p.Glu1901Ter
ENST00000377833.10:c.5701G>T MANE Select ENSP00000367064.4:p.Glu1901Ter
NM_001081.3:c.5701G>T , LRG_540t1:c.5701G>T NP_001072.2:p.Glu1901Ter
ENST00000377833.8:c.5701G>T ENSP00000367064.4:p.Glu1901Ter
XM_011519708.1:c.5701G>T XP_011518010.1:p.Glu1901Ter
XM_011519708.2:c.5701G>T XP_011518010.1:p.Glu1901Ter
XM_011519709.1:c.1687G>T XP_011518011.1:p.Glu563Ter
XM_011519709.2:c.1687G>T XP_011518011.1:p.Glu563Ter
XM_011519710.1:c.1663G>T XP_011518012.1:p.Glu555Ter
XM_011519710.2:c.1663G>T XP_011518012.1:p.Glu555Ter
XM_011519711.1:c.1543G>T XP_011518013.1:p.Glu515Ter
XM_011519711.3:c.1543G>T XP_011518013.1:p.Glu515Ter