Canonical Allele Identifier: CA203559624

Gene: CUBN

Linked Data - Variant Effect Evidence

Linked Data - Sequence & Population

Linked Data - NCBI & NCI

Genomic Alleles

HGVS	Genome Assembly
NC_000010.11:g.16863501C>G , CM000672.2:g.16863501C>G	GRCh38
NC_000010.10:g.16905500C>G , CM000672.1:g.16905500C>G	GRCh37
NC_000010.9:g.16945506C>G	NCBI36
NG_008967.1:g.271317G>C , LRG_540:g.271317G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000377833.10:c.9454+6135G>C MANE Select	ENSP00000367064.4:n.9454+6135G>C
ENST00000649135.1:n.49+3306G>C
ENST00000377833.8:c.9454+6135G>C	ENSP00000367064.4:n.9454+6135G>C
NM_001081.3:c.9454+6135G>C , LRG_540t1:c.9454+6135G>C	NP_001072.2:n.9454+6135G>C
XM_011519709.1:c.5440+6135G>C	XP_011518011.1:n.5440+6135G>C
XM_011519710.1:c.5416+6135G>C	XP_011518012.1:n.5416+6135G>C
XM_011519711.1:c.5296+6135G>C	XP_011518013.1:n.5296+6135G>C
XM_011519709.2:c.5440+6135G>C	XP_011518011.1:n.5440+6135G>C
XM_011519710.2:c.5416+6135G>C	XP_011518012.1:n.5416+6135G>C
XM_011519711.3:c.5296+6135G>C	XP_011518013.1:n.5296+6135G>C
NM_001081.4:c.9454+6135G>C MANE Select	NP_001072.2:n.9454+6135G>C