Canonical Allele Identifier: CA2682436063
Gene: NME8 HGNC NCBI
EPDR1 HGNC NCBI

Linked Data

gnomAD v4: 7-37862002-C-A
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000007.14:g.37862002C>A , CM000669.2:g.37862002C>A GRCh38
NC_000007.13:g.37901604C>A , CM000669.1:g.37901604C>A GRCh37
NC_000007.12:g.37868129C>A NCBI36
NG_015893.1:g.18406C>A

Transcript Alleles

HGVS Amino-acid change
ENST00000199447.9:c.271-26C>A (NME8) MANE Select ENSP00000199447.4:n.271-26C>A
ENST00000199447.8:c.271-26C>A (NME8) ENSP00000199447.4:n.271-26C>A
ENST00000426106.1:c.105+4657C>A (NME8) ENSP00000408841.1:n.105+4657C>A
ENST00000440017.5:c.271-26C>A (NME8) ENSP00000397063.1:n.271-26C>A
ENST00000444718.5:c.106-26C>A (NME8) ENSP00000390596.1:n.106-26C>A
ENST00000455500.5:c.106-26C>A (NME8) ENSP00000390047.1:n.106-26C>A
ENST00000476620.1:c.-38+4657C>A (EPDR1) ENSP00000425858.1:n.-38+4657C>A
NM_016616.4:c.271-26C>A (NME8) NP_057700.3:n.271-26C>A
NM_016616.5:c.271-26C>A (NME8) MANE Select NP_057700.3:n.271-26C>A
Search 100 bp 5'
Search 100 bp 3'