Canonical Allele Identifier: CA376145968

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16957831T>G (hg19) ; chr10:g.16915832T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915832T>G , CM000672.2:g.16915832T>G	GRCh38
NC_000010.10:g.16957831T>G , CM000672.1:g.16957831T>G	GRCh37
NC_000010.9:g.16997837T>G	NCBI36
NG_008967.1:g.218986A>C , LRG_540:g.218986A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7199A>C MANE Select	ENSP00000367064.4:p.Asn2400Thr
ENST00000377833.8:c.7199A>C	ENSP00000367064.4:p.Asn2400Thr
NM_001081.3:c.7199A>C , LRG_540t1:c.7199A>C	NP_001072.2:p.Asn2400Thr
XM_011519708.1:c.7199A>C	XP_011518010.1:p.Asn2400Thr
XM_011519709.1:c.3185A>C	XP_011518011.1:p.Asn1062Thr
XM_011519710.1:c.3161A>C	XP_011518012.1:p.Asn1054Thr
XM_011519711.1:c.3041A>C	XP_011518013.1:p.Asn1014Thr
XM_011519708.2:c.7199A>C	XP_011518010.1:p.Asn2400Thr
XM_011519709.2:c.3185A>C	XP_011518011.1:p.Asn1062Thr
XM_011519710.2:c.3161A>C	XP_011518012.1:p.Asn1054Thr
XM_011519711.3:c.3041A>C	XP_011518013.1:p.Asn1014Thr
NM_001081.4:c.7199A>C MANE Select	NP_001072.2:p.Asn2400Thr