Canonical Allele Identifier: CA2680371798
Gene: ENPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890617del , CM000668.2:g.131890617del GRCh38
NC_000006.11:g.132211757del , CM000668.1:g.132211757del GRCh37
NC_000006.10:g.132253450del NCBI36
NG_008206.1:g.87602del

Transcript Alleles

HGVS Amino-acid Change
ENST00000684674.1:n.1315del
ENST00000647893.1:c.*106del MANE Select ENSP00000498074.1:n.*106del
ENST00000360971.6:c.*106del ENSP00000354238.2:n.*106del
ENST00000513998.5:c.*1721del ENSP00000422424.1:n.*1721del
NM_006208.2:c.*106del NP_006199.2:n.*106del
XM_011535896.1:c.*106del XP_011534198.1:n.*106del
NM_006208.3:c.*106del MANE Select NP_006199.2:n.*106del