Canonical Allele Identifier: CA203531313

Gene: CUBN

Linked Data

• dbSNP Id: rs929744737
• gnomAD v3: 10-16824843-T-C
• gnomAD v4: 10-16824843-T-C
• MyVariant Identifiers: chr10:g.16866842T>C (hg19) ; chr10:g.16824843T>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16824843T>C , CM000672.2:g.16824843T>C	GRCh38
NC_000010.10:g.16866842T>C , CM000672.1:g.16866842T>C	GRCh37
NC_000010.9:g.16906848T>C	NCBI36
NG_008967.1:g.309975A>G , LRG_540:g.309975A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.*132A>G MANE Select	ENSP00000367064.4:n.*132A>G
ENST00000377833.8:c.*132A>G	ENSP00000367064.4:n.*132A>G
NM_001081.3:c.*132A>G , LRG_540t1:c.*132A>G	NP_001072.2:n.*132A>G
XM_011519709.1:c.*132A>G	XP_011518011.1:n.*132A>G
XM_011519710.1:c.*132A>G	XP_011518012.1:n.*132A>G
XM_011519711.1:c.*132A>G	XP_011518013.1:n.*132A>G
XM_011519709.2:c.*132A>G	XP_011518011.1:n.*132A>G
XM_011519710.2:c.*132A>G	XP_011518012.1:n.*132A>G
XM_011519711.3:c.*132A>G	XP_011518013.1:n.*132A>G
NM_001081.4:c.*132A>G MANE Select	NP_001072.2:n.*132A>G