Canonical Allele Identifier: CA1664276990
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131876985T= , CM000668.2:g.131876985T= GRCh38
NC_000006.11:g.132198125T= , CM000668.1:g.132198125T= GRCh37
NC_000006.10:g.132239818T= NCBI36
NG_008206.1:g.73970T=

Transcript Alleles

HGVS Amino-acid Change
ENST00000683687.1:n.596-7T=
ENST00000684536.1:n.222-7T=
ENST00000647893.1:c.1724-7T= MANE Select ENSP00000498074.1:n.1724-7T=
ENST00000647981.1:n.409-7T=
ENST00000650437.1:c.1215-7T=
ENST00000360971.6:c.1724-7T= ENSP00000354238.2:n.1724-7T=
ENST00000459624.1:n.768-7T=
ENST00000513998.5:c.*561-7T= ENSP00000422424.1:n.*561-7T=
NM_006208.2:c.1724-7T= NP_006199.2:n.1724-7T=
XM_011535896.1:c.614-7T= XP_011534198.1:n.614-7T=
NM_006208.3:c.1724-7T= MANE Select NP_006199.2:n.1724-7T=