Canonical Allele Identifier: CA177500

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37850714C>T , CM000669.2:g.37850714C>T GRCh38
NC_000007.13:g.37890316C>T , CM000669.1:g.37890316C>T GRCh37
NC_000007.12:g.37856841C>T NCBI36
NG_015893.1:g.7118C>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000199447.9:c.177C>T (NME8) MANE Select ENSP00000199447.4:p.Asp59=
ENST00000199447.8:c.177C>T (NME8) ENSP00000199447.4:p.Asp59=
ENST00000426106.1:c.33+415C>T (NME8) ENSP00000408841.1:n.33+415C>T
ENST00000440017.5:c.177C>T (NME8) ENSP00000397063.1:p.Asp59=
ENST00000444718.5:c.33+415C>T (NME8) ENSP00000390596.1:n.33+415C>T
ENST00000455500.5:c.33+415C>T (NME8) ENSP00000390047.1:n.33+415C>T
ENST00000476620.1:c.-109-6560C>T (EPDR1) ENSP00000425858.1:n.-109-6560C>T
NM_016616.4:c.177C>T (NME8) NP_057700.3:p.Asp59=
NM_016616.5:c.177C>T (NME8) MANE Select NP_057700.3:p.Asp59=