Canonical Allele Identifier: CA203550587

Gene: CUBN

Linked Data

• dbSNP Id: rs111280023
• MyVariant Identifiers: chr10:g.16997778C>G (hg19) ; chr10:g.16955779C>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16955779C>G , CM000672.2:g.16955779C>G	GRCh38
NC_000010.10:g.16997778C>G , CM000672.1:g.16997778C>G	GRCh37
NC_000010.9:g.17037784C>G	NCBI36
NG_008967.1:g.179039G>C , LRG_540:g.179039G>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.4696-1231G>C MANE Select	ENSP00000367064.4:n.4696-1231G>C
ENST00000377833.8:c.4696-1231G>C	ENSP00000367064.4:n.4696-1231G>C
NM_001081.3:c.4696-1231G>C , LRG_540t1:c.4696-1231G>C	NP_001072.2:n.4696-1231G>C
XM_011519708.1:c.4696-1231G>C	XP_011518010.1:n.4696-1231G>C
XM_011519709.1:c.682-1231G>C	XP_011518011.1:n.682-1231G>C
XM_011519710.1:c.658-1231G>C	XP_011518012.1:n.658-1231G>C
XM_011519711.1:c.538-1231G>C	XP_011518013.1:n.538-1231G>C
XM_011519708.2:c.4696-1231G>C	XP_011518010.1:n.4696-1231G>C
XM_011519709.2:c.682-1231G>C	XP_011518011.1:n.682-1231G>C
XM_011519710.2:c.658-1231G>C	XP_011518012.1:n.658-1231G>C
XM_011519711.3:c.538-1231G>C	XP_011518013.1:n.538-1231G>C
NM_001081.4:c.4696-1231G>C MANE Select	NP_001072.2:n.4696-1231G>C