Canonical Allele Identifier: CA1664260055
Gene: ENPP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131861508G= , CM000668.2:g.131861508G= GRCh38
NC_000006.11:g.132182648G= , CM000668.1:g.132182648G= GRCh37
NC_000006.10:g.132224341G= NCBI36
NG_008206.1:g.58493G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.916-87G= MANE Select ENSP00000498074.1:n.916-87G=
ENST00000650147.1:c.533-87G=
ENST00000650437.1:c.407-87G=
ENST00000360971.6:c.916-87G= ENSP00000354238.2:n.916-87G=
ENST00000513998.5:c.916-87G= ENSP00000422424.1:n.916-87G=
NM_006208.2:c.916-87G= NP_006199.2:n.916-87G=
NM_006208.3:c.916-87G= MANE Select NP_006199.2:n.916-87G=
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