Canonical Allele Identifier: CA1664240760
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1781628445

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131832659C>G , CM000668.2:g.131832659C>G GRCh38
NC_000006.11:g.132153799C>G , CM000668.1:g.132153799C>G GRCh37
NC_000006.10:g.132195492C>G NCBI36
NG_008206.1:g.29644C>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647893.1:c.241-15117C>G MANE Select ENSP00000498074.1:n.241-15117C>G
ENST00000650507.1:c.247+6544C>G ENSP00000497375.1:n.247+6544C>G
ENST00000360971.6:c.241-15117C>G ENSP00000354238.2:n.241-15117C>G
ENST00000486853.1:n.261-15117C>G
ENST00000513998.5:c.241-15117C>G ENSP00000422424.1:n.241-15117C>G
NM_006208.2:c.241-15117C>G NP_006199.2:n.241-15117C>G
NM_006208.3:c.241-15117C>G MANE Select NP_006199.2:n.241-15117C>G