Canonical Allele Identifier: CA300657932

Gene: DCC

Linked Data

• dbSNP Id: rs574694659
• gnomAD v2: 18-50432222-C-CT
• gnomAD v3: 18-52905852-C-CT
• gnomAD v4: 18-52905852-C-CT
• MyVariant Identifiers: chr18:g.50432222_50432223insT (hg19) ; chr18:g.52905852_52905853insT (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52905857dup , CM000680.2:g.52905857dup	GRCh38
NC_000018.9:g.50432227dup , CM000680.1:g.50432227dup	GRCh37
NC_000018.8:g.48686225dup	NCBI36
NG_013341.1:g.570686dup
NG_013341.2:g.570686dup

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.413-187dup MANE Select	ENSP00000389140.2:n.413-187dup
ENST00000304775.12:c.214-187dup
ENST00000412726.5:c.344-187dup	ENSP00000397322.2:n.344-187dup
ENST00000442544.6:c.413-187dup	ENSP00000389140.2:n.413-187dup
ENST00000579349.1:c.334-187dup
ENST00000580024.1:n.326-187dup
ENST00000581559.1:c.334-187dup	ENSP00000463463.1:n.334-187dup
NM_005215.3:c.413-187dup	NP_005206.2:n.413-187dup
XM_011525843.1:c.413-187dup	XP_011524145.1:n.413-187dup
XM_011525845.1:c.413-187dup	XP_011524147.1:n.413-187dup
XM_011525846.1:c.413-187dup	XP_011524148.1:n.413-187dup
XM_017025568.1:c.413-187dup	XP_016881057.1:n.413-187dup
XM_017025569.1:c.413-187dup	XP_016881058.1:n.413-187dup
NM_005215.4:c.413-187dup MANE Select	NP_005206.2:n.413-187dup