Canonical Allele Identifier: CA376146098
Gene: CUBN HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16915853T>G , CM000672.2:g.16915853T>G GRCh38
NC_000010.10:g.16957852T>G , CM000672.1:g.16957852T>G GRCh37
NC_000010.9:g.16997858T>G NCBI36
NG_008967.1:g.218965A>C , LRG_540:g.218965A>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.7178A>C MANE Select ENSP00000367064.4:p.Asp2393Ala
ENST00000377833.8:c.7178A>C ENSP00000367064.4:p.Asp2393Ala
NM_001081.3:c.7178A>C , LRG_540t1:c.7178A>C NP_001072.2:p.Asp2393Ala
XM_011519708.1:c.7178A>C XP_011518010.1:p.Asp2393Ala
XM_011519709.1:c.3164A>C XP_011518011.1:p.Asp1055Ala
XM_011519710.1:c.3140A>C XP_011518012.1:p.Asp1047Ala
XM_011519711.1:c.3020A>C XP_011518013.1:p.Asp1007Ala
XM_011519708.2:c.7178A>C XP_011518010.1:p.Asp2393Ala
XM_011519709.2:c.3164A>C XP_011518011.1:p.Asp1055Ala
XM_011519710.2:c.3140A>C XP_011518012.1:p.Asp1047Ala
XM_011519711.3:c.3020A>C XP_011518013.1:p.Asp1007Ala
NM_001081.4:c.7178A>C MANE Select NP_001072.2:p.Asp2393Ala