Canonical Allele Identifier: CA2680366330
Gene: ENPP1 HGNC NCBI

Linked Data

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131851112_131851120del , CM000668.2:g.131851112_131851120del GRCh38
NC_000006.11:g.132172252_132172260del , CM000668.1:g.132172252_132172260del GRCh37
NC_000006.10:g.132213945_132213953del NCBI36
NG_008206.1:g.48097_48105del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.431-30_431-22del MANE Select ENSP00000498074.1:n.431-30_431-22del
ENST00000650147.1:c.109-30_109-22del
ENST00000650437.1:c.108+1006_108+1014del
ENST00000360971.6:c.431-30_431-22del ENSP00000354238.2:n.431-30_431-22del
ENST00000486853.1:n.451-30_451-22del
ENST00000513998.5:c.431-30_431-22del ENSP00000422424.1:n.431-30_431-22del
NM_006208.2:c.431-30_431-22del NP_006199.2:n.431-30_431-22del
NM_006208.3:c.431-30_431-22del MANE Select NP_006199.2:n.431-30_431-22del