Canonical Allele Identifier: CA2735262678

Gene: DCC

Linked Data

• dbSNP Id: rs2144958290

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52665938_52665940del , CM000680.2:g.52665938_52665940del	GRCh38
NC_000018.9:g.50192308_50192310del , CM000680.1:g.50192308_50192310del	GRCh37
NC_000018.8:g.48446306_48446308del	NCBI36
NG_013341.1:g.330767_330769del
NG_013341.2:g.330767_330769del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.92-86116_92-86114del MANE Select	ENSP00000389140.2:n.92-86116_92-86114del
ENST00000442544.6:c.92-86116_92-86114del	ENSP00000389140.2:n.92-86116_92-86114del
NM_005215.3:c.92-86116_92-86114del	NP_005206.2:n.92-86116_92-86114del
XM_011525843.1:c.92-86116_92-86114del	XP_011524145.1:n.92-86116_92-86114del
XM_011525845.1:c.92-86116_92-86114del	XP_011524147.1:n.92-86116_92-86114del
XM_011525846.1:c.92-86116_92-86114del	XP_011524148.1:n.92-86116_92-86114del
XM_017025568.1:c.92-86116_92-86114del	XP_016881057.1:n.92-86116_92-86114del
XM_017025569.1:c.92-86116_92-86114del	XP_016881058.1:n.92-86116_92-86114del
NM_005215.4:c.92-86116_92-86114del MANE Select	NP_005206.2:n.92-86116_92-86114del