Canonical Allele Identifier: CA503875773

Gene: DCC

Linked Data

• MyVariant Identifiers: chr18:g.50918146T>C (hg19)

Genomic Alleles

HGVS	Genome Assembly
NC_000018.10:g.53391776T>C , CM000680.2:g.53391776T>C	GRCh38
NC_000018.9:g.50918146T>C , CM000680.1:g.50918146T>C	GRCh37
NC_000018.8:g.49172144T>C	NCBI36
NG_013341.1:g.1056605T>C
NG_013341.2:g.1056605T>C

Transcript Alleles

HGVS	Amino-acid change
ENST00000442544.7:c.2577T>C MANE Select	ENSP00000389140.2:p.Ala859=
ENST00000304775.12:c.2257-5532T>C
ENST00000412726.5:c.2508T>C	ENSP00000397322.2:p.Ala836=
ENST00000442544.6:c.2577T>C	ENSP00000389140.2:p.Ala859=
ENST00000581580.5:c.1482T>C	ENSP00000464582.1:p.Ala494=
NM_005215.3:c.2577T>C	NP_005206.2:p.Ala859=
XM_011525843.1:c.2577T>C	XP_011524145.1:p.Ala859=
XM_011525844.1:c.1542T>C	XP_011524146.1:p.Ala514=
XM_011525845.1:c.2577T>C	XP_011524147.1:p.Ala859=
XM_011525846.1:c.2517T>C	XP_011524148.1:p.Ala839=
XM_011525844.2:c.1542T>C	XP_011524146.1:p.Ala514=
XM_017025568.1:c.2577T>C	XP_016881057.1:p.Ala859=
XM_017025569.1:c.2517T>C	XP_016881058.1:p.Ala839=
XM_017025570.1:c.1542T>C	XP_016881059.1:p.Ala514=
NM_005215.4:c.2577T>C MANE Select	NP_005206.2:p.Ala859=