Canonical Allele Identifier: CA4222126

Gene: NME8 EPDR1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.37861979G>A , CM000669.2:g.37861979G>A	GRCh38
NC_000007.13:g.37901581G>A , CM000669.1:g.37901581G>A	GRCh37
NC_000007.12:g.37868106G>A	NCBI36
NG_015893.1:g.18383G>A

Transcript Alleles

HGVS	Amino-acid Change
NM_016616.5:c.271-49G>A (NME8) MANE Select	NP_057700.3:n.271-49G>A
ENST00000199447.9:c.271-49G>A (NME8) MANE Select	ENSP00000199447.4:n.271-49G>A
NM_016616.4:c.271-49G>A (NME8)	NP_057700.3:n.271-49G>A
ENST00000199447.8:c.271-49G>A (NME8)	ENSP00000199447.4:n.271-49G>A
ENST00000426106.1:c.105+4634G>A (NME8)	ENSP00000408841.1:n.105+4634G>A
ENST00000440017.5:c.271-49G>A (NME8)	ENSP00000397063.1:n.271-49G>A
ENST00000444718.5:c.106-49G>A (NME8)	ENSP00000390596.1:n.106-49G>A
ENST00000455500.5:c.106-49G>A (NME8)	ENSP00000390047.1:n.106-49G>A
ENST00000476620.1:c.-38+4634G>A (EPDR1)	ENSP00000425858.1:n.-38+4634G>A