Canonical Allele Identifier: CA2713033575
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs2114737287

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890616_131890626del , CM000668.2:g.131890616_131890626del GRCh38
NC_000006.11:g.132211756_132211766del , CM000668.1:g.132211756_132211766del GRCh37
NC_000006.10:g.132253449_132253459del NCBI36
NG_008206.1:g.87601_87611del

Transcript Alleles

HGVS Amino-acid Change
ENST00000684674.1:n.1314_1324del
ENST00000647893.1:c.*105_*115del MANE Select ENSP00000498074.1:n.*105_*115del
ENST00000360971.6:c.*105_*115del ENSP00000354238.2:n.*105_*115del
ENST00000513998.5:c.*1720_*1730del ENSP00000422424.1:n.*1720_*1730del
NM_006208.2:c.*105_*115del NP_006199.2:n.*105_*115del
XM_011535896.1:c.*105_*115del XP_011534198.1:n.*105_*115del
NM_006208.3:c.*105_*115del MANE Select NP_006199.2:n.*105_*115del