Canonical Allele Identifier: CA1664240785
Gene: ENPP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131832700T= , CM000668.2:g.131832700T= GRCh38
NC_000006.11:g.132153840T= , CM000668.1:g.132153840T= GRCh37
NC_000006.10:g.132195533T= NCBI36
NG_008206.1:g.29685T=

Transcript Alleles

HGVS Amino-acid change
ENST00000647893.1:c.241-15076T= MANE Select ENSP00000498074.1:n.241-15076T=
ENST00000650507.1:c.247+6585T= ENSP00000497375.1:n.247+6585T=
ENST00000360971.6:c.241-15076T= ENSP00000354238.2:n.241-15076T=
ENST00000486853.1:n.261-15076T=
ENST00000513998.5:c.241-15076T= ENSP00000422424.1:n.241-15076T=
NM_006208.2:c.241-15076T= NP_006199.2:n.241-15076T=
NM_006208.3:c.241-15076T= MANE Select NP_006199.2:n.241-15076T=
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