Canonical Allele Identifier: CA468298478

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16867001G>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16825002G>C , CM000672.2:g.16825002G>C	GRCh38
NC_000010.10:g.16867001G>C , CM000672.1:g.16867001G>C	GRCh37
NC_000010.9:g.16907007G>C	NCBI36
NG_008967.1:g.309816C>G , LRG_540:g.309816C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.10845C>G MANE Select	ENSP00000367064.4:p.Ser3615=
ENST00000377833.8:c.10845C>G	ENSP00000367064.4:p.Ser3615=
NM_001081.3:c.10845C>G , LRG_540t1:c.10845C>G	NP_001072.2:p.Ser3615=
XM_011519709.1:c.6831C>G	XP_011518011.1:p.Ser2277=
XM_011519710.1:c.6807C>G	XP_011518012.1:p.Ser2269=
XM_011519711.1:c.6687C>G	XP_011518013.1:p.Ser2229=
XM_011519709.2:c.6831C>G	XP_011518011.1:p.Ser2277=
XM_011519710.2:c.6807C>G	XP_011518012.1:p.Ser2269=
XM_011519711.3:c.6687C>G	XP_011518013.1:p.Ser2229=
NM_001081.4:c.10845C>G MANE Select	NP_001072.2:p.Ser3615=