Canonical Allele Identifier: CA1664277023
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131877063G= , CM000668.2:g.131877063G= GRCh38
NC_000006.11:g.132198203G= , CM000668.1:g.132198203G= GRCh37
NC_000006.10:g.132239896G= NCBI36
NG_008206.1:g.74048G=

Transcript Alleles

HGVS Amino-acid change
ENST00000683687.1:n.667G=
ENST00000684536.1:n.293G=
ENST00000647893.1:c.1795G= MANE Select ENSP00000498074.1:p.Val599=
ENST00000647981.1:n.480G=
ENST00000650437.1:c.1286G=
ENST00000360971.6:c.1795G= ENSP00000354238.2:p.Val599=
ENST00000459624.1:n.839G=
ENST00000513998.5:c.*632G= ENSP00000422424.1:n.*632G=
NM_006208.2:c.1795G= NP_006199.2:p.Val599=
XM_011535896.1:c.685G= XP_011534198.1:p.Val229=
NM_006208.3:c.1795G= MANE Select NP_006199.2:p.Val599=