Canonical Allele Identifier: CA1664237901
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1781581692
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131829242C>T , CM000668.2:g.131829242C>T GRCh38
NC_000006.11:g.132150382C>T , CM000668.1:g.132150382C>T GRCh37
NC_000006.10:g.132192075C>T NCBI36
NG_008206.1:g.26227C>T

Transcript Alleles

HGVS Amino-acid change
ENST00000647893.1:c.241-18534C>T MANE Select ENSP00000498074.1:n.241-18534C>T
ENST00000650507.1:c.247+3127C>T ENSP00000497375.1:n.247+3127C>T
ENST00000360971.6:c.241-18534C>T ENSP00000354238.2:n.241-18534C>T
ENST00000486853.1:n.261-18534C>T
ENST00000513998.5:c.241-18534C>T ENSP00000422424.1:n.241-18534C>T
NM_006208.2:c.241-18534C>T NP_006199.2:n.241-18534C>T
NM_006208.3:c.241-18534C>T MANE Select NP_006199.2:n.241-18534C>T
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