Canonical Allele Identifier: CA1664253835
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1781879863
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131851422T>A , CM000668.2:g.131851422T>A GRCh38
NC_000006.11:g.132172562T>A , CM000668.1:g.132172562T>A GRCh37
NC_000006.10:g.132214255T>A NCBI36
NG_008206.1:g.48407T>A

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.556+155T>A MANE Select ENSP00000498074.1:n.556+155T>A
ENST00000650147.1:c.234+155T>A
ENST00000650437.1:c.108+1316T>A
ENST00000360971.6:c.556+155T>A ENSP00000354238.2:n.556+155T>A
ENST00000486853.1:n.731T>A
ENST00000513998.5:c.556+155T>A ENSP00000422424.1:n.556+155T>A
NM_006208.2:c.556+155T>A NP_006199.2:n.556+155T>A
NM_006208.3:c.556+155T>A MANE Select NP_006199.2:n.556+155T>A
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