Canonical Allele Identifier: CA1664260074
Gene: ENPP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131861536C= , CM000668.2:g.131861536C= GRCh38
NC_000006.11:g.132182676C= , CM000668.1:g.132182676C= GRCh37
NC_000006.10:g.132224369C= NCBI36
NG_008206.1:g.58521C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.916-59C= MANE Select ENSP00000498074.1:n.916-59C=
ENST00000650147.1:c.533-59C=
ENST00000650437.1:c.407-59C=
ENST00000360971.6:c.916-59C= ENSP00000354238.2:n.916-59C=
ENST00000513998.5:c.916-59C= ENSP00000422424.1:n.916-59C=
NM_006208.2:c.916-59C= NP_006199.2:n.916-59C=
NM_006208.3:c.916-59C= MANE Select NP_006199.2:n.916-59C=
Search 100 bp 5'
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