Canonical Allele Identifier: CA629976438

Gene: DCC

Linked Data

• dbSNP Id: rs1289327999
• gnomAD v2: 18-50734218-A-G
• gnomAD v4: 18-53207848-A-G
• MyVariant Identifiers: chr18:g.50734218A>G (hg19) ; chr18:g.53207848A>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53207848A>G , CM000680.2:g.53207848A>G	GRCh38
NC_000018.9:g.50734218A>G , CM000680.1:g.50734218A>G	GRCh37
NC_000018.8:g.48988216A>G	NCBI36
NG_013341.1:g.872677A>G
NG_013341.2:g.872677A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.1861+31A>G MANE Select	ENSP00000389140.2:n.1861+31A>G
ENST00000304775.12:c.1662+31A>G
ENST00000412726.5:c.1792+31A>G	ENSP00000397322.2:n.1792+31A>G
ENST00000442544.6:c.1861+31A>G	ENSP00000389140.2:n.1861+31A>G
ENST00000581580.5:c.826+31A>G	ENSP00000464582.1:n.826+31A>G
NM_005215.3:c.1861+31A>G	NP_005206.2:n.1861+31A>G
XM_011525843.1:c.1861+31A>G	XP_011524145.1:n.1861+31A>G
XM_011525844.1:c.826+31A>G	XP_011524146.1:n.826+31A>G
XM_011525845.1:c.1861+31A>G	XP_011524147.1:n.1861+31A>G
XM_011525846.1:c.1861+31A>G	XP_011524148.1:n.1861+31A>G
XM_011525844.2:c.826+31A>G	XP_011524146.1:n.826+31A>G
XM_017025568.1:c.1861+31A>G	XP_016881057.1:n.1861+31A>G
XM_017025569.1:c.1861+31A>G	XP_016881058.1:n.1861+31A>G
XM_017025570.1:c.826+31A>G	XP_016881059.1:n.826+31A>G
NM_005215.4:c.1861+31A>G MANE Select	NP_005206.2:n.1861+31A>G