Canonical Allele Identifier: CA2735223461

Gene: DCC

Linked Data

• dbSNP Id: rs2144558781

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53207726del , CM000680.2:g.53207726del	GRCh38
NC_000018.9:g.50734096del , CM000680.1:g.50734096del	GRCh37
NC_000018.8:g.48988094del	NCBI36
NG_013341.1:g.872555del
NG_013341.2:g.872555del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.1770del MANE Select	ENSP00000389140.2:p.Lys590AsnfsTer10
ENST00000304775.12:c.1571del
ENST00000412726.5:c.1701del	ENSP00000397322.2:p.Lys567AsnfsTer10
ENST00000442544.6:c.1770del	ENSP00000389140.2:p.Lys590AsnfsTer10
ENST00000581580.5:c.735del	ENSP00000464582.1:p.Lys245AsnfsTer10
NM_005215.3:c.1770del	NP_005206.2:p.Lys590AsnfsTer10
XM_011525843.1:c.1770del	XP_011524145.1:p.Lys590AsnfsTer10
XM_011525844.1:c.735del	XP_011524146.1:p.Lys245AsnfsTer10
XM_011525845.1:c.1770del	XP_011524147.1:p.Lys590AsnfsTer10
XM_011525846.1:c.1770del	XP_011524148.1:p.Lys590AsnfsTer10
XM_011525844.2:c.735del	XP_011524146.1:p.Lys245AsnfsTer10
XM_017025568.1:c.1770del	XP_016881057.1:p.Lys590AsnfsTer10
XM_017025569.1:c.1770del	XP_016881058.1:p.Lys590AsnfsTer10
XM_017025570.1:c.735del	XP_016881059.1:p.Lys245AsnfsTer10
NM_005215.4:c.1770del MANE Select	NP_005206.2:p.Lys590AsnfsTer10