Canonical Allele Identifier: CA147909690
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs78472543

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131829203A>G , CM000668.2:g.131829203A>G GRCh38
NC_000006.11:g.132150343A>G , CM000668.1:g.132150343A>G GRCh37
NC_000006.10:g.132192036A>G NCBI36
NG_008206.1:g.26188A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.241-18573A>G MANE Select ENSP00000498074.1:n.241-18573A>G
ENST00000650507.1:c.247+3088A>G ENSP00000497375.1:n.247+3088A>G
ENST00000360971.6:c.241-18573A>G ENSP00000354238.2:n.241-18573A>G
ENST00000486853.1:n.261-18573A>G
ENST00000513998.5:c.241-18573A>G ENSP00000422424.1:n.241-18573A>G
NM_006208.2:c.241-18573A>G NP_006199.2:n.241-18573A>G
NM_006208.3:c.241-18573A>G MANE Select NP_006199.2:n.241-18573A>G