Canonical Allele Identifier: CA662288815

Gene: CUBN

Linked Data

• dbSNP Id: rs1261732482
• gnomAD v3: 10-16824748-G-C
• gnomAD v4: 10-16824748-G-C
• MyVariant Identifiers: chr10:g.16866747G>C (hg19) ; chr10:g.16824748G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16824748G>C , CM000672.2:g.16824748G>C	GRCh38
NC_000010.10:g.16866747G>C , CM000672.1:g.16866747G>C	GRCh37
NC_000010.9:g.16906753G>C	NCBI36
NG_008967.1:g.310070C>G , LRG_540:g.310070C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.*227C>G MANE Select	ENSP00000367064.4:n.*227C>G
ENST00000377833.8:c.*227C>G	ENSP00000367064.4:n.*227C>G
NM_001081.3:c.*227C>G , LRG_540t1:c.*227C>G	NP_001072.2:n.*227C>G
XM_011519709.1:c.*227C>G	XP_011518011.1:n.*227C>G
XM_011519710.1:c.*227C>G	XP_011518012.1:n.*227C>G
XM_011519711.1:c.*227C>G	XP_011518013.1:n.*227C>G
XM_011519709.2:c.*227C>G	XP_011518011.1:n.*227C>G
XM_011519710.2:c.*227C>G	XP_011518012.1:n.*227C>G
XM_011519711.3:c.*227C>G	XP_011518013.1:n.*227C>G
NM_001081.4:c.*227C>G MANE Select	NP_001072.2:n.*227C>G