Canonical Allele Identifier: CA376146734

Gene: CUBN

Linked Data

• MyVariant Identifiers: chr10:g.16957966A>G (hg19) ; chr10:g.16915967A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16915967A>G , CM000672.2:g.16915967A>G	GRCh38
NC_000010.10:g.16957966A>G , CM000672.1:g.16957966A>G	GRCh37
NC_000010.9:g.16997972A>G	NCBI36
NG_008967.1:g.218851T>C , LRG_540:g.218851T>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.7064T>C MANE Select	ENSP00000367064.4:p.Leu2355Pro
ENST00000377833.8:c.7064T>C	ENSP00000367064.4:p.Leu2355Pro
NM_001081.3:c.7064T>C , LRG_540t1:c.7064T>C	NP_001072.2:p.Leu2355Pro
XM_011519708.1:c.7064T>C	XP_011518010.1:p.Leu2355Pro
XM_011519709.1:c.3050T>C	XP_011518011.1:p.Leu1017Pro
XM_011519710.1:c.3026T>C	XP_011518012.1:p.Leu1009Pro
XM_011519711.1:c.2906T>C	XP_011518013.1:p.Leu969Pro
XM_011519708.2:c.7064T>C	XP_011518010.1:p.Leu2355Pro
XM_011519709.2:c.3050T>C	XP_011518011.1:p.Leu1017Pro
XM_011519710.2:c.3026T>C	XP_011518012.1:p.Leu1009Pro
XM_011519711.3:c.2906T>C	XP_011518013.1:p.Leu969Pro
NM_001081.4:c.7064T>C MANE Select	NP_001072.2:p.Leu2355Pro