Canonical Allele Identifier: CA1100330573

Gene: NME8 EPDR1

Linked Data

• dbSNP Id: rs1784603419
• gnomAD v3: 7-37862000-TC-T
• gnomAD v4: 7-37862000-TC-T

Genomic Alleles

HGVS	Genome Assembly
NC_000007.14:g.37862004del , CM000669.2:g.37862004del	GRCh38
NC_000007.13:g.37901606del , CM000669.1:g.37901606del	GRCh37
NC_000007.12:g.37868131del	NCBI36
NG_015893.1:g.18408del

Transcript Alleles

HGVS	Amino-acid change
ENST00000199447.9:c.271-24del (NME8) MANE Select	ENSP00000199447.4:n.271-24del
ENST00000199447.8:c.271-24del (NME8)	ENSP00000199447.4:n.271-24del
ENST00000426106.1:c.105+4659del (NME8)	ENSP00000408841.1:n.105+4659del
ENST00000440017.5:c.271-24del (NME8)	ENSP00000397063.1:n.271-24del
ENST00000444718.5:c.106-24del (NME8)	ENSP00000390596.1:n.106-24del
ENST00000455500.5:c.106-24del (NME8)	ENSP00000390047.1:n.106-24del
ENST00000476620.1:c.-38+4659del (EPDR1)	ENSP00000425858.1:n.-38+4659del
NM_016616.4:c.271-24del (NME8)	NP_057700.3:n.271-24del
NM_016616.5:c.271-24del (NME8) MANE Select	NP_057700.3:n.271-24del