Canonical Allele Identifier: CA376146154

Gene: CUBN

Linked Data

• gnomAD v4: 10-16915862-C-G
• MyVariant Identifiers: chr10:g.16957861C>G (hg19) ; chr10:g.16915862C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915862C>G , CM000672.2:g.16915862C>G	GRCh38
NC_000010.10:g.16957861C>G , CM000672.1:g.16957861C>G	GRCh37
NC_000010.9:g.16997867C>G	NCBI36
NG_008967.1:g.218956G>C , LRG_540:g.218956G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.7169G>C MANE Select	ENSP00000367064.4:p.Cys2390Ser
ENST00000377833.8:c.7169G>C	ENSP00000367064.4:p.Cys2390Ser
NM_001081.3:c.7169G>C , LRG_540t1:c.7169G>C	NP_001072.2:p.Cys2390Ser
XM_011519708.1:c.7169G>C	XP_011518010.1:p.Cys2390Ser
XM_011519709.1:c.3155G>C	XP_011518011.1:p.Cys1052Ser
XM_011519710.1:c.3131G>C	XP_011518012.1:p.Cys1044Ser
XM_011519711.1:c.3011G>C	XP_011518013.1:p.Cys1004Ser
XM_011519708.2:c.7169G>C	XP_011518010.1:p.Cys2390Ser
XM_011519709.2:c.3155G>C	XP_011518011.1:p.Cys1052Ser
XM_011519710.2:c.3131G>C	XP_011518012.1:p.Cys1044Ser
XM_011519711.3:c.3011G>C	XP_011518013.1:p.Cys1004Ser
NM_001081.4:c.7169G>C MANE Select	NP_001072.2:p.Cys2390Ser