Canonical Allele Identifier: CA5422484
Gene: CUBN HGNC NCBI
ClinVar Variation:
gnomAD v4:
MyVariant.info:

Genomic Alleles

HGVS Genome Assembly
NC_000010.11:g.16836338C>G , CM000672.2:g.16836338C>G GRCh38
NC_000010.10:g.16878337C>G , CM000672.1:g.16878337C>G GRCh37
NC_000010.9:g.16918343C>G NCBI36
NG_008967.1:g.298480G>C , LRG_540:g.298480G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000377833.10:c.10077G>C MANE Select ENSP00000367064.4:p.Ser3359=
ENST00000377833.8:c.10077G>C ENSP00000367064.4:p.Ser3359=
NM_001081.3:c.10077G>C , LRG_540t1:c.10077G>C NP_001072.2:p.Ser3359=
XM_011519709.1:c.6063G>C XP_011518011.1:p.Ser2021=
XM_011519710.1:c.6039G>C XP_011518012.1:p.Ser2013=
XM_011519711.1:c.5919G>C XP_011518013.1:p.Ser1973=
XM_011519709.2:c.6063G>C XP_011518011.1:p.Ser2021=
XM_011519710.2:c.6039G>C XP_011518012.1:p.Ser2013=
XM_011519711.3:c.5919G>C XP_011518013.1:p.Ser1973=
NM_001081.4:c.10077G>C MANE Select NP_001072.2:p.Ser3359=