Canonical Allele Identifier: CA780383556

Gene: DCC

Linked Data

• dbSNP Id: rs1451569079
• gnomAD v3: 18-52905778-CTTTG-C
• gnomAD v4: 18-52905778-CTTTG-C
• MyVariant Identifiers: chr18:g.50432149_50432152del (hg19) ; chr18:g.52905779_52905782del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52905782_52905785del , CM000680.2:g.52905782_52905785del	GRCh38
NC_000018.9:g.50432152_50432155del , CM000680.1:g.50432152_50432155del	GRCh37
NC_000018.8:g.48686150_48686153del	NCBI36
NG_013341.1:g.570611_570614del
NG_013341.2:g.570611_570614del

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.413-262_413-259del MANE Select	ENSP00000389140.2:n.413-262_413-259del
ENST00000304775.12:c.214-262_214-259del
ENST00000412726.5:c.344-262_344-259del	ENSP00000397322.2:n.344-262_344-259del
ENST00000442544.6:c.413-262_413-259del	ENSP00000389140.2:n.413-262_413-259del
ENST00000579349.1:c.334-262_334-259del
ENST00000580024.1:n.326-262_326-259del
ENST00000581559.1:c.334-262_334-259del	ENSP00000463463.1:n.334-262_334-259del
NM_005215.3:c.413-262_413-259del	NP_005206.2:n.413-262_413-259del
XM_011525843.1:c.413-262_413-259del	XP_011524145.1:n.413-262_413-259del
XM_011525845.1:c.413-262_413-259del	XP_011524147.1:n.413-262_413-259del
XM_011525846.1:c.413-262_413-259del	XP_011524148.1:n.413-262_413-259del
XM_017025568.1:c.413-262_413-259del	XP_016881057.1:n.413-262_413-259del
XM_017025569.1:c.413-262_413-259del	XP_016881058.1:n.413-262_413-259del
NM_005215.4:c.413-262_413-259del MANE Select	NP_005206.2:n.413-262_413-259del