Canonical Allele Identifier: CA2303874880

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52905778_52905782delinsCTTTG , CM000680.2:g.52905778_52905782delinsCTTTG	GRCh38
NC_000018.9:g.50432148_50432152delinsCTTTG , CM000680.1:g.50432148_50432152delinsCTTTG	GRCh37
NC_000018.8:g.48686146_48686150delinsCTTTG	NCBI36
NG_013341.1:g.570607_570611delinsCTTTG
NG_013341.2:g.570607_570611delinsCTTTG

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.413-266_413-262delinsCTTTG MANE Select	ENSP00000389140.2:n.413-266_413-262delinsCTTTG
ENST00000304775.12:c.214-266_214-262delinsCTTTG
ENST00000412726.5:c.344-266_344-262delinsCTTTG	ENSP00000397322.2:n.344-266_344-262delinsCTTTG
ENST00000442544.6:c.413-266_413-262delinsCTTTG	ENSP00000389140.2:n.413-266_413-262delinsCTTTG
ENST00000579349.1:c.334-266_334-262delinsCTTTG
ENST00000580024.1:n.326-266_326-262delinsCTTTG
ENST00000581559.1:c.334-266_334-262delinsCTTTG	ENSP00000463463.1:n.334-266_334-262delinsCTTTG
NM_005215.3:c.413-266_413-262delinsCTTTG	NP_005206.2:n.413-266_413-262delinsCTTTG
XM_011525843.1:c.413-266_413-262delinsCTTTG	XP_011524145.1:n.413-266_413-262delinsCTTTG
XM_011525845.1:c.413-266_413-262delinsCTTTG	XP_011524147.1:n.413-266_413-262delinsCTTTG
XM_011525846.1:c.413-266_413-262delinsCTTTG	XP_011524148.1:n.413-266_413-262delinsCTTTG
XM_017025568.1:c.413-266_413-262delinsCTTTG	XP_016881057.1:n.413-266_413-262delinsCTTTG
XM_017025569.1:c.413-266_413-262delinsCTTTG	XP_016881058.1:n.413-266_413-262delinsCTTTG
NM_005215.4:c.413-266_413-262delinsCTTTG MANE Select	NP_005206.2:n.413-266_413-262delinsCTTTG