Canonical Allele Identifier: CA658658754

Gene: DCC

Linked Data

• ClinVar Variation Id: 446724
• ClinVar RCV Id: RCV000494700
• dbSNP Id: rs1555682265
• MyVariant Identifiers: chr18:g.50450167_50450173del (hg19) ; chr18:g.52923797_52923803del (hg38)
• PubMed: PMID:28250456

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52923797_52923803del , CM000680.2:g.52923797_52923803del	GRCh38
NC_000018.9:g.50450167_50450173del , CM000680.1:g.50450167_50450173del	GRCh37
NC_000018.8:g.48704165_48704171del	NCBI36
NG_013341.1:g.588626_588632del
NG_013341.2:g.588626_588632del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.788_794del MANE Select	ENSP00000389140.2:p.Val263AlafsTer?
ENST00000304775.12:c.589_595del
ENST00000412726.5:c.719_725del	ENSP00000397322.2:p.Val240AlafsTer?
ENST00000442544.6:c.788_794del	ENSP00000389140.2:p.Val263AlafsTer?
ENST00000584710.5:n.14_20del
NM_005215.3:c.788_794del	NP_005206.2:p.Val263AlafsTer?
XM_011525843.1:c.788_794del	XP_011524145.1:p.Val263AlafsTer?
XM_011525845.1:c.788_794del	XP_011524147.1:p.Val263AlafsTer?
XM_011525846.1:c.788_794del	XP_011524148.1:p.Val263AlafsTer?
XM_017025568.1:c.788_794del	XP_016881057.1:p.Val263AlafsTer?
XM_017025569.1:c.788_794del	XP_016881058.1:p.Val263AlafsTer?
NM_005215.4:c.788_794del MANE Select	NP_005206.2:p.Val263AlafsTer?