Canonical Allele Identifier: CA1664253762
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131851247A= , CM000668.2:g.131851247A= GRCh38
NC_000006.11:g.132172387A= , CM000668.1:g.132172387A= GRCh37
NC_000006.10:g.132214080A= NCBI36
NG_008206.1:g.48232A=

Transcript Alleles

HGVS Amino-acid change
ENST00000647893.1:c.536A= MANE Select ENSP00000498074.1:p.Asn179=
ENST00000650147.1:c.214A=
ENST00000650437.1:c.108+1141A=
ENST00000360971.6:c.536A= ENSP00000354238.2:p.Asn179=
ENST00000486853.1:n.556A=
ENST00000513998.5:c.536A= ENSP00000422424.1:p.Asn179=
NM_006208.2:c.536A= NP_006199.2:p.Asn179=
NM_006208.3:c.536A= MANE Select NP_006199.2:p.Asn179=