Canonical Allele Identifier: CA503999512

Gene: DCC

Linked Data

• MyVariant Identifiers: chr18:g.50432667A>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.52906297A>G , CM000680.2:g.52906297A>G	GRCh38
NC_000018.9:g.50432667A>G , CM000680.1:g.50432667A>G	GRCh37
NC_000018.8:g.48686665A>G	NCBI36
NG_013341.1:g.571126A>G
NG_013341.2:g.571126A>G

Transcript Alleles

HGVS	Amino-acid Change
ENST00000442544.7:c.666A>G MANE Select	ENSP00000389140.2:p.Thr222=
ENST00000304775.12:c.467A>G
ENST00000412726.5:c.597A>G	ENSP00000397322.2:p.Thr199=
ENST00000442544.6:c.666A>G	ENSP00000389140.2:p.Thr222=
NM_005215.3:c.666A>G	NP_005206.2:p.Thr222=
XM_011525843.1:c.666A>G	XP_011524145.1:p.Thr222=
XM_011525845.1:c.666A>G	XP_011524147.1:p.Thr222=
XM_011525846.1:c.666A>G	XP_011524148.1:p.Thr222=
XM_017025568.1:c.666A>G	XP_016881057.1:p.Thr222=
XM_017025569.1:c.666A>G	XP_016881058.1:p.Thr222=
NM_005215.4:c.666A>G MANE Select	NP_005206.2:p.Thr222=