Canonical Allele Identifier: CA1700779285
Gene: NME8 HGNC NCBI
EPDR1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37888364G= , CM000669.2:g.37888364G= GRCh38
NC_000007.13:g.37927966G= , CM000669.1:g.37927966G= GRCh37
NC_000007.12:g.37894491G= NCBI36
NG_015893.1:g.44768G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000199447.9:c.1335G= (NME8) MANE Select ENSP00000199447.4:p.Gln445=
ENST00000199447.8:c.1335G= (NME8) ENSP00000199447.4:p.Gln445=
ENST00000426106.1:c.*281G= (NME8) ENSP00000408841.1:n.*281G=
ENST00000440017.5:c.1335G= (NME8) ENSP00000397063.1:p.Gln445=
ENST00000476620.1:c.-38+31019G= (EPDR1) ENSP00000425858.1:n.-38+31019G=
NM_016616.4:c.1335G= (NME8) NP_057700.3:p.Gln445=
NM_016616.5:c.1335G= (NME8) MANE Select NP_057700.3:p.Gln445=
Search 100 bp 5'
Search 100 bp 3'