Canonical Allele Identifier: CA402471680

Gene: DCC

Linked Data

• MyVariant Identifiers: chr18:g.50912469G>T (hg19) ; chr18:g.53386099G>T (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53386099G>T , CM000680.2:g.53386099G>T	GRCh38
NC_000018.9:g.50912469G>T , CM000680.1:g.50912469G>T	GRCh37
NC_000018.8:g.49166467G>T	NCBI36
NG_013341.1:g.1050928G>T
NG_013341.2:g.1050928G>T

Transcript Alleles

HGVS	Amino-acid change
ENST00000442544.7:c.2416G>T MANE Select	ENSP00000389140.2:p.Val806Phe
ENST00000304775.12:c.2217G>T
ENST00000412726.5:c.2347G>T	ENSP00000397322.2:p.Val783Phe
ENST00000442544.6:c.2416G>T	ENSP00000389140.2:p.Val806Phe
ENST00000581580.5:c.1381G>T	ENSP00000464582.1:p.Val461Phe
NM_005215.3:c.2416G>T	NP_005206.2:p.Val806Phe
XM_011525843.1:c.2416G>T	XP_011524145.1:p.Val806Phe
XM_011525844.1:c.1381G>T	XP_011524146.1:p.Val461Phe
XM_011525845.1:c.2416G>T	XP_011524147.1:p.Val806Phe
XM_011525846.1:c.2416G>T	XP_011524148.1:p.Val806Phe
XM_011525844.2:c.1381G>T	XP_011524146.1:p.Val461Phe
XM_017025568.1:c.2416G>T	XP_016881057.1:p.Val806Phe
XM_017025569.1:c.2416G>T	XP_016881058.1:p.Val806Phe
XM_017025570.1:c.1381G>T	XP_016881059.1:p.Val461Phe
NM_005215.4:c.2416G>T MANE Select	NP_005206.2:p.Val806Phe