Canonical Allele Identifier: CA147912126
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs962622413
gnomAD v2: 6-132153996-G-C
gnomAD v3: 6-131832856-G-C
gnomAD v4: 6-131832856-G-C
MyVariant Identifiers: chr6:g.132153996G>C (hg19) chr6:g.131832856G>C (hg38)
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131832856G>C , CM000668.2:g.131832856G>C GRCh38
NC_000006.11:g.132153996G>C , CM000668.1:g.132153996G>C GRCh37
NC_000006.10:g.132195689G>C NCBI36
NG_008206.1:g.29841G>C

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.241-14920G>C MANE Select ENSP00000498074.1:n.241-14920G>C
ENST00000650507.1:c.247+6741G>C ENSP00000497375.1:n.247+6741G>C
ENST00000360971.6:c.241-14920G>C ENSP00000354238.2:n.241-14920G>C
ENST00000486853.1:n.261-14920G>C
ENST00000513998.5:c.241-14920G>C ENSP00000422424.1:n.241-14920G>C
NM_006208.2:c.241-14920G>C NP_006199.2:n.241-14920G>C
NM_006208.3:c.241-14920G>C MANE Select NP_006199.2:n.241-14920G>C
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