Canonical Allele Identifier: CA2581350215
Community Standard Title: NM_005215.4(DCC):c.*275A>T
Gene: DCC HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000018.10:g.53530928A>T , CM000680.2:g.53530928A>T GRCh38
NC_000018.9:g.51057298A>T , CM000680.1:g.51057298A>T GRCh37
NC_000018.8:g.49311296A>T NCBI36
NG_013341.1:g.1195757A>T
NG_013341.2:g.1195757A>T

Transcript Alleles

HGVS Amino-acid Change
NM_005215.4:c.*275A>T MANE Select NP_005206.2:n.*275A>T
ENST00000442544.7:c.*275A>T MANE Select ENSP00000389140.2:n.*275A>T
NM_005215.3:c.*275A>T NP_005206.2:n.*275A>T
ENST00000412726.5:c.4550A>T ENSP00000397322.2:n.4550A>T
ENST00000442544.6:c.*275A>T ENSP00000389140.2:n.*275A>T
XM_011525844.1:c.*275A>T XP_011524146.1:n.*275A>T
XM_011525844.2:c.*275A>T XP_011524146.1:n.*275A>T
XM_017025568.1:c.*275A>T XP_016881057.1:n.*275A>T
XM_017025569.1:c.*275A>T XP_016881058.1:n.*275A>T
XM_017025570.1:c.*275A>T XP_016881059.1:n.*275A>T