Canonical Allele Identifier: CA2304037706

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53207890_53207895delinsTATATC , CM000680.2:g.53207890_53207895delinsTATATC	GRCh38
NC_000018.9:g.50734260_50734265delinsTATATC , CM000680.1:g.50734260_50734265delinsTATATC	GRCh37
NC_000018.8:g.48988258_48988263delinsTATATC	NCBI36
NG_013341.1:g.872719_872724delinsTATATC
NG_013341.2:g.872719_872724delinsTATATC

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.1861+73_1861+78delinsTATATC MANE Select	ENSP00000389140.2:n.1861+73_1861+78delinsTATATC
ENST00000304775.12:c.1662+73_1662+78delinsTATATC
ENST00000412726.5:c.1792+73_1792+78delinsTATATC	ENSP00000397322.2:n.1792+73_1792+78delinsTATATC
ENST00000442544.6:c.1861+73_1861+78delinsTATATC	ENSP00000389140.2:n.1861+73_1861+78delinsTATATC
ENST00000581580.5:c.826+73_826+78delinsTATATC	ENSP00000464582.1:n.826+73_826+78delinsTATATC
NM_005215.3:c.1861+73_1861+78delinsTATATC	NP_005206.2:n.1861+73_1861+78delinsTATATC
XM_011525843.1:c.1861+73_1861+78delinsTATATC	XP_011524145.1:n.1861+73_1861+78delinsTATATC
XM_011525844.1:c.826+73_826+78delinsTATATC	XP_011524146.1:n.826+73_826+78delinsTATATC
XM_011525845.1:c.1861+73_1861+78delinsTATATC	XP_011524147.1:n.1861+73_1861+78delinsTATATC
XM_011525846.1:c.1861+73_1861+78delinsTATATC	XP_011524148.1:n.1861+73_1861+78delinsTATATC
XM_011525844.2:c.826+73_826+78delinsTATATC	XP_011524146.1:n.826+73_826+78delinsTATATC
XM_017025568.1:c.1861+73_1861+78delinsTATATC	XP_016881057.1:n.1861+73_1861+78delinsTATATC
XM_017025569.1:c.1861+73_1861+78delinsTATATC	XP_016881058.1:n.1861+73_1861+78delinsTATATC
XM_017025570.1:c.826+73_826+78delinsTATATC	XP_016881059.1:n.826+73_826+78delinsTATATC
NM_005215.4:c.1861+73_1861+78delinsTATATC MANE Select	NP_005206.2:n.1861+73_1861+78delinsTATATC