Canonical Allele Identifier: CA503999416

Gene: DCC

Linked Data

• MyVariant Identifiers: chr18:g.50432598C>A (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52906228C>A , CM000680.2:g.52906228C>A	GRCh38
NC_000018.9:g.50432598C>A , CM000680.1:g.50432598C>A	GRCh37
NC_000018.8:g.48686596C>A	NCBI36
NG_013341.1:g.571057C>A
NG_013341.2:g.571057C>A

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.597C>A MANE Select	ENSP00000389140.2:p.Ile199=
ENST00000304775.12:c.398C>A
ENST00000412726.5:c.528C>A	ENSP00000397322.2:p.Ile176=
ENST00000442544.6:c.597C>A	ENSP00000389140.2:p.Ile199=
ENST00000579349.1:c.518C>A
ENST00000580024.1:n.510C>A
ENST00000581559.1:c.518C>A	ENSP00000463463.1:n.518C>A
NM_005215.3:c.597C>A	NP_005206.2:p.Ile199=
XM_011525843.1:c.597C>A	XP_011524145.1:p.Ile199=
XM_011525845.1:c.597C>A	XP_011524147.1:p.Ile199=
XM_011525846.1:c.597C>A	XP_011524148.1:p.Ile199=
XM_017025568.1:c.597C>A	XP_016881057.1:p.Ile199=
XM_017025569.1:c.597C>A	XP_016881058.1:p.Ile199=
NM_005215.4:c.597C>A MANE Select	NP_005206.2:p.Ile199=