Canonical Allele Identifier: CA402471582

Gene: DCC

Linked Data

• COSMIC: COSM5608271 ; COSM5608272
• MyVariant Identifiers: chr18:g.50912426T>A (hg19) ; chr18:g.53386056T>A (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53386056T>A , CM000680.2:g.53386056T>A	GRCh38
NC_000018.9:g.50912426T>A , CM000680.1:g.50912426T>A	GRCh37
NC_000018.8:g.49166424T>A	NCBI36
NG_013341.1:g.1050885T>A
NG_013341.2:g.1050885T>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.2373T>A MANE Select	ENSP00000389140.2:p.His791Gln
ENST00000304775.12:c.2174T>A
ENST00000412726.5:c.2304T>A	ENSP00000397322.2:p.His768Gln
ENST00000442544.6:c.2373T>A	ENSP00000389140.2:p.His791Gln
ENST00000581580.5:c.1338T>A	ENSP00000464582.1:p.His446Gln
NM_005215.3:c.2373T>A	NP_005206.2:p.His791Gln
XM_011525843.1:c.2373T>A	XP_011524145.1:p.His791Gln
XM_011525844.1:c.1338T>A	XP_011524146.1:p.His446Gln
XM_011525845.1:c.2373T>A	XP_011524147.1:p.His791Gln
XM_011525846.1:c.2373T>A	XP_011524148.1:p.His791Gln
XM_011525844.2:c.1338T>A	XP_011524146.1:p.His446Gln
XM_017025568.1:c.2373T>A	XP_016881057.1:p.His791Gln
XM_017025569.1:c.2373T>A	XP_016881058.1:p.His791Gln
XM_017025570.1:c.1338T>A	XP_016881059.1:p.His446Gln
NM_005215.4:c.2373T>A MANE Select	NP_005206.2:p.His791Gln