Canonical Allele Identifier: CA2578870082
Gene: NME8 HGNC NCBI
EPDR1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37888243_37888244del , CM000669.2:g.37888243_37888244del GRCh38
NC_000007.13:g.37927845_37927846del , CM000669.1:g.37927845_37927846del GRCh37
NC_000007.12:g.37894370_37894371del NCBI36
NG_015893.1:g.44647_44648del

Transcript Alleles

HGVS Amino-acid change
ENST00000199447.9:c.1248-34_1248-33del (NME8) MANE Select ENSP00000199447.4:n.1248-34_1248-33del
ENST00000199447.8:c.1248-34_1248-33del (NME8) ENSP00000199447.4:n.1248-34_1248-33del
ENST00000426106.1:c.*194-34_*194-33del (NME8) ENSP00000408841.1:n.*194-34_*194-33del
ENST00000440017.5:c.1248-34_1248-33del (NME8) ENSP00000397063.1:n.1248-34_1248-33del
ENST00000476620.1:c.-38+30898_-38+30899del (EPDR1) ENSP00000425858.1:n.-38+30898_-38+30899de...
NM_016616.4:c.1248-34_1248-33del (NME8) NP_057700.3:n.1248-34_1248-33del
NM_016616.5:c.1248-34_1248-33del (NME8) MANE Select NP_057700.3:n.1248-34_1248-33del
Search 100 bp 5'
Search 100 bp 3'