Canonical Allele Identifier: CA376145931

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16957825G>C (hg19) ; chr10:g.16915826G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915826G>C , CM000672.2:g.16915826G>C	GRCh38
NC_000010.10:g.16957825G>C , CM000672.1:g.16957825G>C	GRCh37
NC_000010.9:g.16997831G>C	NCBI36
NG_008967.1:g.218992C>G , LRG_540:g.218992C>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7205C>G MANE Select	ENSP00000367064.4:p.Thr2402Ser
ENST00000377833.8:c.7205C>G	ENSP00000367064.4:p.Thr2402Ser
NM_001081.3:c.7205C>G , LRG_540t1:c.7205C>G	NP_001072.2:p.Thr2402Ser
XM_011519708.1:c.7205C>G	XP_011518010.1:p.Thr2402Ser
XM_011519709.1:c.3191C>G	XP_011518011.1:p.Thr1064Ser
XM_011519710.1:c.3167C>G	XP_011518012.1:p.Thr1056Ser
XM_011519711.1:c.3047C>G	XP_011518013.1:p.Thr1016Ser
XM_011519708.2:c.7205C>G	XP_011518010.1:p.Thr2402Ser
XM_011519709.2:c.3191C>G	XP_011518011.1:p.Thr1064Ser
XM_011519710.2:c.3167C>G	XP_011518012.1:p.Thr1056Ser
XM_011519711.3:c.3047C>G	XP_011518013.1:p.Thr1016Ser
NM_001081.4:c.7205C>G MANE Select	NP_001072.2:p.Thr2402Ser