Canonical Allele Identifier: CA367219585

Gene: NME8 EPDR1

Linked Data

• MyVariant Identifiers: chr7:g.37890304A>C (hg19) ; chr7:g.37850702A>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.37850702A>C , CM000669.2:g.37850702A>C	GRCh38
NC_000007.13:g.37890304A>C , CM000669.1:g.37890304A>C	GRCh37
NC_000007.12:g.37856829A>C	NCBI36
NG_015893.1:g.7106A>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000199447.9:c.165A>C (NME8) MANE Select	ENSP00000199447.4:p.Glu55Asp
ENST00000199447.8:c.165A>C (NME8)	ENSP00000199447.4:p.Glu55Asp
ENST00000426106.1:c.33+403A>C (NME8)	ENSP00000408841.1:n.33+403A>C
ENST00000440017.5:c.165A>C (NME8)	ENSP00000397063.1:p.Glu55Asp
ENST00000444718.5:c.33+403A>C (NME8)	ENSP00000390596.1:n.33+403A>C
ENST00000455500.5:c.33+403A>C (NME8)	ENSP00000390047.1:n.33+403A>C
ENST00000476620.1:c.-109-6572A>C (EPDR1)	ENSP00000425858.1:n.-109-6572A>C
NM_016616.4:c.165A>C (NME8)	NP_057700.3:p.Glu55Asp
NM_016616.5:c.165A>C (NME8) MANE Select	NP_057700.3:p.Glu55Asp