Canonical Allele Identifier: CA147912098
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs752764170

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131832849_131832851del , CM000668.2:g.131832849_131832851del GRCh38
NC_000006.11:g.132153989_132153991del , CM000668.1:g.132153989_132153991del GRCh37
NC_000006.10:g.132195682_132195684del NCBI36
NG_008206.1:g.29834_29836del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.241-14927_241-14925del MANE Select ENSP00000498074.1:n.241-14927_241-14925del
ENST00000650507.1:c.247+6734_247+6736del ENSP00000497375.1:n.247+6734_247+6736del
ENST00000360971.6:c.241-14927_241-14925del ENSP00000354238.2:n.241-14927_241-14925del
ENST00000486853.1:n.261-14927_261-14925del
ENST00000513998.5:c.241-14927_241-14925del ENSP00000422424.1:n.241-14927_241-14925del
NM_006208.2:c.241-14927_241-14925del NP_006199.2:n.241-14927_241-14925del
NM_006208.3:c.241-14927_241-14925del MANE Select NP_006199.2:n.241-14927_241-14925del