Canonical Allele Identifier: CA2303874987

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52906023_52906026delinsCCTT , CM000680.2:g.52906023_52906026delinsCCTT	GRCh38
NC_000018.9:g.50432393_50432396delinsCCTT , CM000680.1:g.50432393_50432396delinsCCTT	GRCh37
NC_000018.8:g.48686391_48686394delinsCCTT	NCBI36
NG_013341.1:g.570852_570855delinsCCTT
NG_013341.2:g.570852_570855delinsCCTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.413-21_413-18delinsCCTT MANE Select	ENSP00000389140.2:n.413-21_413-18delinsCCTT
ENST00000304775.12:c.214-21_214-18delinsCCTT
ENST00000412726.5:c.344-21_344-18delinsCCTT	ENSP00000397322.2:n.344-21_344-18delinsCCTT
ENST00000442544.6:c.413-21_413-18delinsCCTT	ENSP00000389140.2:n.413-21_413-18delinsCCTT
ENST00000579349.1:c.334-21_334-18delinsCCTT
ENST00000580024.1:n.326-21_326-18delinsCCTT
ENST00000581559.1:c.334-21_334-18delinsCCTT	ENSP00000463463.1:n.334-21_334-18delinsCCTT
NM_005215.3:c.413-21_413-18delinsCCTT	NP_005206.2:n.413-21_413-18delinsCCTT
XM_011525843.1:c.413-21_413-18delinsCCTT	XP_011524145.1:n.413-21_413-18delinsCCTT
XM_011525845.1:c.413-21_413-18delinsCCTT	XP_011524147.1:n.413-21_413-18delinsCCTT
XM_011525846.1:c.413-21_413-18delinsCCTT	XP_011524148.1:n.413-21_413-18delinsCCTT
XM_017025568.1:c.413-21_413-18delinsCCTT	XP_016881057.1:n.413-21_413-18delinsCCTT
XM_017025569.1:c.413-21_413-18delinsCCTT	XP_016881058.1:n.413-21_413-18delinsCCTT
NM_005215.4:c.413-21_413-18delinsCCTT MANE Select	NP_005206.2:n.413-21_413-18delinsCCTT