Canonical Allele Identifier: CA300690472

Gene: DCC

Linked Data

• dbSNP Id: rs780391157
• gnomAD v4: 18-53385923-ATTCT-A
• MyVariant Identifiers: chr18:g.50912294_50912297del (hg19) ; chr18:g.53385924_53385927del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53385925_53385928del , CM000680.2:g.53385925_53385928del	GRCh38
NC_000018.9:g.50912295_50912298del , CM000680.1:g.50912295_50912298del	GRCh37
NC_000018.8:g.49166293_49166296del	NCBI36
NG_013341.1:g.1050754_1050757del
NG_013341.2:g.1050754_1050757del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.2360-118_2360-115del MANE Select	ENSP00000389140.2:n.2360-118_2360-115del
ENST00000304775.12:c.2161-118_2161-115del
ENST00000412726.5:c.2291-118_2291-115del	ENSP00000397322.2:n.2291-118_2291-115del
ENST00000442544.6:c.2360-118_2360-115del	ENSP00000389140.2:n.2360-118_2360-115del
ENST00000581580.5:c.1325-118_1325-115del	ENSP00000464582.1:n.1325-118_1325-115del
NM_005215.3:c.2360-118_2360-115del	NP_005206.2:n.2360-118_2360-115del
XM_011525843.1:c.2360-118_2360-115del	XP_011524145.1:n.2360-118_2360-115del
XM_011525844.1:c.1325-118_1325-115del	XP_011524146.1:n.1325-118_1325-115del
XM_011525845.1:c.2360-118_2360-115del	XP_011524147.1:n.2360-118_2360-115del
XM_011525846.1:c.2360-118_2360-115del	XP_011524148.1:n.2360-118_2360-115del
XM_011525844.2:c.1325-118_1325-115del	XP_011524146.1:n.1325-118_1325-115del
XM_017025568.1:c.2360-118_2360-115del	XP_016881057.1:n.2360-118_2360-115del
XM_017025569.1:c.2360-118_2360-115del	XP_016881058.1:n.2360-118_2360-115del
XM_017025570.1:c.1325-118_1325-115del	XP_016881059.1:n.1325-118_1325-115del
NM_005215.4:c.2360-118_2360-115del MANE Select	NP_005206.2:n.2360-118_2360-115del