Canonical Allele Identifier: CA402513913

Gene: DCC

Linked Data

• MyVariant Identifiers: chr18:g.50432628T>G (hg19) ; chr18:g.52906258T>G (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52906258T>G , CM000680.2:g.52906258T>G	GRCh38
NC_000018.9:g.50432628T>G , CM000680.1:g.50432628T>G	GRCh37
NC_000018.8:g.48686626T>G	NCBI36
NG_013341.1:g.571087T>G
NG_013341.2:g.571087T>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.627T>G MANE Select	ENSP00000389140.2:p.Ile209Met
ENST00000304775.12:c.428T>G
ENST00000412726.5:c.558T>G	ENSP00000397322.2:p.Ile186Met
ENST00000442544.6:c.627T>G	ENSP00000389140.2:p.Ile209Met
ENST00000579349.1:c.548T>G
ENST00000580024.1:n.540T>G
NM_005215.3:c.627T>G	NP_005206.2:p.Ile209Met
XM_011525843.1:c.627T>G	XP_011524145.1:p.Ile209Met
XM_011525845.1:c.627T>G	XP_011524147.1:p.Ile209Met
XM_011525846.1:c.627T>G	XP_011524148.1:p.Ile209Met
XM_017025568.1:c.627T>G	XP_016881057.1:p.Ile209Met
XM_017025569.1:c.627T>G	XP_016881058.1:p.Ile209Met
NM_005215.4:c.627T>G MANE Select	NP_005206.2:p.Ile209Met