Canonical Allele Identifier: CA1664253702
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131851093C= , CM000668.2:g.131851093C= GRCh38
NC_000006.11:g.132172233C= , CM000668.1:g.132172233C= GRCh37
NC_000006.10:g.132213926C= NCBI36
NG_008206.1:g.48078C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.431-49C= MANE Select ENSP00000498074.1:n.431-49C=
ENST00000650147.1:c.109-49C=
ENST00000650437.1:c.108+987C=
ENST00000360971.6:c.431-49C= ENSP00000354238.2:n.431-49C=
ENST00000486853.1:n.451-49C=
ENST00000513998.5:c.431-49C= ENSP00000422424.1:n.431-49C=
NM_006208.2:c.431-49C= NP_006199.2:n.431-49C=
NM_006208.3:c.431-49C= MANE Select NP_006199.2:n.431-49C=