Canonical Allele Identifier: CA2304129443

Gene: DCC

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53385975_53385977delinsGTT , CM000680.2:g.53385975_53385977delinsGTT	GRCh38
NC_000018.9:g.50912345_50912347delinsGTT , CM000680.1:g.50912345_50912347delinsGTT	GRCh37
NC_000018.8:g.49166343_49166345delinsGTT	NCBI36
NG_013341.1:g.1050804_1050806delinsGTT
NG_013341.2:g.1050804_1050806delinsGTT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.2360-68_2360-66delinsGTT MANE Select	ENSP00000389140.2:n.2360-68_2360-66delinsGTT
ENST00000304775.12:c.2161-68_2161-66delinsGTT
ENST00000412726.5:c.2291-68_2291-66delinsGTT	ENSP00000397322.2:n.2291-68_2291-66delinsGTT
ENST00000442544.6:c.2360-68_2360-66delinsGTT	ENSP00000389140.2:n.2360-68_2360-66delinsGTT
ENST00000581580.5:c.1325-68_1325-66delinsGTT	ENSP00000464582.1:n.1325-68_1325-66delinsGTT
NM_005215.3:c.2360-68_2360-66delinsGTT	NP_005206.2:n.2360-68_2360-66delinsGTT
XM_011525843.1:c.2360-68_2360-66delinsGTT	XP_011524145.1:n.2360-68_2360-66delinsGTT
XM_011525844.1:c.1325-68_1325-66delinsGTT	XP_011524146.1:n.1325-68_1325-66delinsGTT
XM_011525845.1:c.2360-68_2360-66delinsGTT	XP_011524147.1:n.2360-68_2360-66delinsGTT
XM_011525846.1:c.2360-68_2360-66delinsGTT	XP_011524148.1:n.2360-68_2360-66delinsGTT
XM_011525844.2:c.1325-68_1325-66delinsGTT	XP_011524146.1:n.1325-68_1325-66delinsGTT
XM_017025568.1:c.2360-68_2360-66delinsGTT	XP_016881057.1:n.2360-68_2360-66delinsGTT
XM_017025569.1:c.2360-68_2360-66delinsGTT	XP_016881058.1:n.2360-68_2360-66delinsGTT
XM_017025570.1:c.1325-68_1325-66delinsGTT	XP_016881059.1:n.1325-68_1325-66delinsGTT
NM_005215.4:c.2360-68_2360-66delinsGTT MANE Select	NP_005206.2:n.2360-68_2360-66delinsGTT