Canonical Allele Identifier: CA503999298

Gene: DCC

Linked Data

• MyVariant Identifiers: chr18:g.50432448C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52906078C>A , CM000680.2:g.52906078C>A	GRCh38
NC_000018.9:g.50432448C>A , CM000680.1:g.50432448C>A	GRCh37
NC_000018.8:g.48686446C>A	NCBI36
NG_013341.1:g.570907C>A
NG_013341.2:g.570907C>A

Transcript Alleles

HGVS	Amino-acid change
ENST00000442544.7:c.447C>A MANE Select	ENSP00000389140.2:p.Val149=
ENST00000304775.12:c.248C>A
ENST00000412726.5:c.378C>A	ENSP00000397322.2:p.Val126=
ENST00000442544.6:c.447C>A	ENSP00000389140.2:p.Val149=
ENST00000579349.1:c.368C>A
ENST00000580024.1:n.360C>A
ENST00000581559.1:c.368C>A	ENSP00000463463.1:n.368C>A
NM_005215.3:c.447C>A	NP_005206.2:p.Val149=
XM_011525843.1:c.447C>A	XP_011524145.1:p.Val149=
XM_011525845.1:c.447C>A	XP_011524147.1:p.Val149=
XM_011525846.1:c.447C>A	XP_011524148.1:p.Val149=
XM_017025568.1:c.447C>A	XP_016881057.1:p.Val149=
XM_017025569.1:c.447C>A	XP_016881058.1:p.Val149=
NM_005215.4:c.447C>A MANE Select	NP_005206.2:p.Val149=