Canonical Allele Identifier: CA503875388

Gene: DCC

Linked Data

• MyVariant Identifiers: chr18:g.50912474T>G (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53386104T>G , CM000680.2:g.53386104T>G	GRCh38
NC_000018.9:g.50912474T>G , CM000680.1:g.50912474T>G	GRCh37
NC_000018.8:g.49166472T>G	NCBI36
NG_013341.1:g.1050933T>G
NG_013341.2:g.1050933T>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000442544.7:c.2421T>G MANE Select	ENSP00000389140.2:p.Pro807=
ENST00000304775.12:c.2222T>G
ENST00000412726.5:c.2352T>G	ENSP00000397322.2:p.Pro784=
ENST00000442544.6:c.2421T>G	ENSP00000389140.2:p.Pro807=
ENST00000581580.5:c.1386T>G	ENSP00000464582.1:p.Pro462=
NM_005215.3:c.2421T>G	NP_005206.2:p.Pro807=
XM_011525843.1:c.2421T>G	XP_011524145.1:p.Pro807=
XM_011525844.1:c.1386T>G	XP_011524146.1:p.Pro462=
XM_011525845.1:c.2421T>G	XP_011524147.1:p.Pro807=
XM_011525846.1:c.2421T>G	XP_011524148.1:p.Pro807=
XM_011525844.2:c.1386T>G	XP_011524146.1:p.Pro462=
XM_017025568.1:c.2421T>G	XP_016881057.1:p.Pro807=
XM_017025569.1:c.2421T>G	XP_016881058.1:p.Pro807=
XM_017025570.1:c.1386T>G	XP_016881059.1:p.Pro462=
NM_005215.4:c.2421T>G MANE Select	NP_005206.2:p.Pro807=