Canonical Allele Identifier: CA1700779064

Gene: NME8 EPDR1

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.37888266_37888267delinsCT , CM000669.2:g.37888266_37888267delinsCT	GRCh38
NC_000007.13:g.37927868_37927869delinsCT , CM000669.1:g.37927868_37927869delinsCT	GRCh37
NC_000007.12:g.37894393_37894394delinsCT	NCBI36
NG_015893.1:g.44670_44671delinsCT

Transcript Alleles

HGVS	Amino-acid Change
ENST00000199447.9:c.1248-11_1248-10delinsCT (NME8) MANE Select	ENSP00000199447.4:n.1248-11_1248-10delinsCT
ENST00000199447.8:c.1248-11_1248-10delinsCT (NME8)	ENSP00000199447.4:n.1248-11_1248-10delinsCT
ENST00000426106.1:c.*194-11_*194-10delinsCT (NME8)	ENSP00000408841.1:n.*194-11_*194-10delinsCT
ENST00000440017.5:c.1248-11_1248-10delinsCT (NME8)	ENSP00000397063.1:n.1248-11_1248-10delinsCT
ENST00000476620.1:c.-38+30921_-38+30922delinsCT (EPDR1)	ENSP00000425858.1:n.-38+30921_-38+30922delinsCT
NM_016616.4:c.1248-11_1248-10delinsCT (NME8)	NP_057700.3:n.1248-11_1248-10delinsCT
NM_016616.5:c.1248-11_1248-10delinsCT (NME8) MANE Select	NP_057700.3:n.1248-11_1248-10delinsCT