Canonical Allele Identifier: CA1700773707
Gene: NME8 HGNC NCBI
EPDR1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37862005T= , CM000669.2:g.37862005T= GRCh38
NC_000007.13:g.37901607T= , CM000669.1:g.37901607T= GRCh37
NC_000007.12:g.37868132T= NCBI36
NG_015893.1:g.18409T=

Transcript Alleles

HGVS Amino-acid change
ENST00000199447.9:c.271-23T= (NME8) MANE Select ENSP00000199447.4:n.271-23T=
ENST00000199447.8:c.271-23T= (NME8) ENSP00000199447.4:n.271-23T=
ENST00000426106.1:c.105+4660T= (NME8) ENSP00000408841.1:n.105+4660T=
ENST00000440017.5:c.271-23T= (NME8) ENSP00000397063.1:n.271-23T=
ENST00000444718.5:c.106-23T= (NME8) ENSP00000390596.1:n.106-23T=
ENST00000455500.5:c.106-23T= (NME8) ENSP00000390047.1:n.106-23T=
ENST00000476620.1:c.-38+4660T= (EPDR1) ENSP00000425858.1:n.-38+4660T=
NM_016616.4:c.271-23T= (NME8) NP_057700.3:n.271-23T=
NM_016616.5:c.271-23T= (NME8) MANE Select NP_057700.3:n.271-23T=
Search 100 bp 5'
Search 100 bp 3'