Canonical Allele Identifier: CA402513677
Gene: DCC HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.52906145C>G , CM000680.2:g.52906145C>G GRCh38
NC_000018.9:g.50432515C>G , CM000680.1:g.50432515C>G GRCh37
NC_000018.8:g.48686513C>G NCBI36
NG_013341.1:g.570974C>G
NG_013341.2:g.570974C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000442544.7:c.514C>G MANE Select ENSP00000389140.2:p.His172Asp
ENST00000304775.12:c.315C>G
ENST00000412726.5:c.445C>G ENSP00000397322.2:p.His149Asp
ENST00000442544.6:c.514C>G ENSP00000389140.2:p.His172Asp
ENST00000579349.1:c.435C>G
ENST00000580024.1:n.427C>G
ENST00000581559.1:c.435C>G ENSP00000463463.1:n.435C>G
NM_005215.3:c.514C>G NP_005206.2:p.His172Asp
XM_011525843.1:c.514C>G XP_011524145.1:p.His172Asp
XM_011525845.1:c.514C>G XP_011524147.1:p.His172Asp
XM_011525846.1:c.514C>G XP_011524148.1:p.His172Asp
XM_017025568.1:c.514C>G XP_016881057.1:p.His172Asp
XM_017025569.1:c.514C>G XP_016881058.1:p.His172Asp
NM_005215.4:c.514C>G MANE Select NP_005206.2:p.His172Asp