Canonical Allele Identifier: CA5423717
Community Standard Title: NM_001081.4(CUBN):c.6309C>T (p.Ile2103=)
Gene: CUBN HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16925737G>A , CM000672.2:g.16925737G>A GRCh38
NC_000010.10:g.16967736G>A , CM000672.1:g.16967736G>A GRCh37
NC_000010.9:g.17007742G>A NCBI36
NG_008967.1:g.209081C>T , LRG_540:g.209081C>T

Transcript Alleles

HGVS Amino-acid Change
NM_001081.4:c.6309C>T MANE Select NP_001072.2:p.Ile2103=
ENST00000377833.10:c.6309C>T MANE Select ENSP00000367064.4:p.Ile2103=
NM_001081.3:c.6309C>T , LRG_540t1:c.6309C>T NP_001072.2:p.Ile2103=
ENST00000377833.8:c.6309C>T ENSP00000367064.4:p.Ile2103=
XM_011519708.1:c.6309C>T XP_011518010.1:p.Ile2103=
XM_011519708.2:c.6309C>T XP_011518010.1:p.Ile2103=
XM_011519709.1:c.2295C>T XP_011518011.1:p.Ile765=
XM_011519709.2:c.2295C>T XP_011518011.1:p.Ile765=
XM_011519710.1:c.2271C>T XP_011518012.1:p.Ile757=
XM_011519710.2:c.2271C>T XP_011518012.1:p.Ile757=
XM_011519711.1:c.2151C>T XP_011518013.1:p.Ile717=
XM_011519711.3:c.2151C>T XP_011518013.1:p.Ile717=