Canonical Allele Identifier: CA990396985

Gene: DCC

Linked Data

• ClinVar Variation Id: 2439657
• ClinVar RCV Id: RCV003143908
• dbSNP Id: rs2039877071
• gnomAD v3: 18-52906062-CACAG-C
• gnomAD v4: 18-52906062-CACAG-C

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52906068_52906071del , CM000680.2:g.52906068_52906071del	GRCh38
NC_000018.9:g.50432438_50432441del , CM000680.1:g.50432438_50432441del	GRCh37
NC_000018.8:g.48686436_48686439del	NCBI36
NG_013341.1:g.570897_570900del
NG_013341.2:g.570897_570900del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.437_440del MANE Select	ENSP00000389140.2:p.Thr146AsnfsTer?
ENST00000304775.12:c.238_241del
ENST00000412726.5:c.368_371del	ENSP00000397322.2:p.Thr123AsnfsTer?
ENST00000442544.6:c.437_440del	ENSP00000389140.2:p.Thr146AsnfsTer?
ENST00000579349.1:c.358_361del
ENST00000580024.1:n.350_353del
ENST00000581559.1:c.358_361del	ENSP00000463463.1:n.358_361del
NM_005215.3:c.437_440del	NP_005206.2:p.Thr146AsnfsTer?
XM_011525843.1:c.437_440del	XP_011524145.1:p.Thr146AsnfsTer?
XM_011525845.1:c.437_440del	XP_011524147.1:p.Thr146AsnfsTer?
XM_011525846.1:c.437_440del	XP_011524148.1:p.Thr146AsnfsTer?
XM_017025568.1:c.437_440del	XP_016881057.1:p.Thr146AsnfsTer?
XM_017025569.1:c.437_440del	XP_016881058.1:p.Thr146AsnfsTer?
NM_005215.4:c.437_440del MANE Select	NP_005206.2:p.Thr146AsnfsTer?