Canonical Allele Identifier: CA1664260058
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1585823982
gnomAD v4: 6-131861510-A-T
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131861510A>T , CM000668.2:g.131861510A>T GRCh38
NC_000006.11:g.132182650A>T , CM000668.1:g.132182650A>T GRCh37
NC_000006.10:g.132224343A>T NCBI36
NG_008206.1:g.58495A>T

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.916-85A>T MANE Select ENSP00000498074.1:n.916-85A>T
ENST00000650147.1:c.533-85A>T
ENST00000650437.1:c.407-85A>T
ENST00000360971.6:c.916-85A>T ENSP00000354238.2:n.916-85A>T
ENST00000513998.5:c.916-85A>T ENSP00000422424.1:n.916-85A>T
NM_006208.2:c.916-85A>T NP_006199.2:n.916-85A>T
NM_006208.3:c.916-85A>T MANE Select NP_006199.2:n.916-85A>T
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