Canonical Allele Identifier: CA127073
Gene: DCC HGNC NCBI

Linked Data

ClinVar Variation Id: 17075
ClinVar RCV Id: RCV000018604
dbSNP Id: rs121912967

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.52906134T>C , CM000680.2:g.52906134T>C GRCh38
NC_000018.9:g.50432504T>C , CM000680.1:g.50432504T>C GRCh37
NC_000018.8:g.48686502T>C NCBI36
NG_013341.1:g.570963T>C
NG_013341.2:g.570963T>C

Transcript Alleles

HGVS Amino-acid change
ENST00000442544.7:c.503T>C MANE Select ENSP00000389140.2:p.Met168Thr
ENST00000304775.12:c.304T>C
ENST00000412726.5:c.434T>C ENSP00000397322.2:p.Met145Thr
ENST00000442544.6:c.503T>C ENSP00000389140.2:p.Met168Thr
ENST00000579349.1:c.424T>C
ENST00000580024.1:n.416T>C
ENST00000581559.1:c.424T>C ENSP00000463463.1:n.424T>C
NM_005215.3:c.503T>C NP_005206.2:p.Met168Thr
XM_011525843.1:c.503T>C XP_011524145.1:p.Met168Thr
XM_011525845.1:c.503T>C XP_011524147.1:p.Met168Thr
XM_011525846.1:c.503T>C XP_011524148.1:p.Met168Thr
XM_017025568.1:c.503T>C XP_016881057.1:p.Met168Thr
XM_017025569.1:c.503T>C XP_016881058.1:p.Met168Thr
NM_005215.4:c.503T>C MANE Select NP_005206.2:p.Met168Thr