Canonical Allele Identifier: CA468301657

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16957845C>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915846C>G , CM000672.2:g.16915846C>G	GRCh38
NC_000010.10:g.16957845C>G , CM000672.1:g.16957845C>G	GRCh37
NC_000010.9:g.16997851C>G	NCBI36
NG_008967.1:g.218972G>C , LRG_540:g.218972G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7185G>C MANE Select	ENSP00000367064.4:p.Val2395=
ENST00000377833.8:c.7185G>C	ENSP00000367064.4:p.Val2395=
NM_001081.3:c.7185G>C , LRG_540t1:c.7185G>C	NP_001072.2:p.Val2395=
XM_011519708.1:c.7185G>C	XP_011518010.1:p.Val2395=
XM_011519709.1:c.3171G>C	XP_011518011.1:p.Val1057=
XM_011519710.1:c.3147G>C	XP_011518012.1:p.Val1049=
XM_011519711.1:c.3027G>C	XP_011518013.1:p.Val1009=
XM_011519708.2:c.7185G>C	XP_011518010.1:p.Val2395=
XM_011519709.2:c.3171G>C	XP_011518011.1:p.Val1057=
XM_011519710.2:c.3147G>C	XP_011518012.1:p.Val1049=
XM_011519711.3:c.3027G>C	XP_011518013.1:p.Val1009=
NM_001081.4:c.7185G>C MANE Select	NP_001072.2:p.Val2395=