Canonical Allele Identifier: CA376119795

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16870824A>G (hg19) ; chr10:g.16828825A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16828825A>G , CM000672.2:g.16828825A>G	GRCh38
NC_000010.10:g.16870824A>G , CM000672.1:g.16870824A>G	GRCh37
NC_000010.9:g.16910830A>G	NCBI36
NG_008967.1:g.305993T>C , LRG_540:g.305993T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000377833.10:c.10744T>C MANE Select	ENSP00000367064.4:p.Ser3582Pro
ENST00000377833.8:c.10744T>C	ENSP00000367064.4:p.Ser3582Pro
NM_001081.3:c.10744T>C , LRG_540t1:c.10744T>C	NP_001072.2:p.Ser3582Pro
XM_011519709.1:c.6730T>C	XP_011518011.1:p.Ser2244Pro
XM_011519710.1:c.6706T>C	XP_011518012.1:p.Ser2236Pro
XM_011519711.1:c.6586T>C	XP_011518013.1:p.Ser2196Pro
XM_011519709.2:c.6730T>C	XP_011518011.1:p.Ser2244Pro
XM_011519710.2:c.6706T>C	XP_011518012.1:p.Ser2236Pro
XM_011519711.3:c.6586T>C	XP_011518013.1:p.Ser2196Pro
NM_001081.4:c.10744T>C MANE Select	NP_001072.2:p.Ser3582Pro