Canonical Allele Identifier: CA147922444
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs925691870

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131846781T>G , CM000668.2:g.131846781T>G GRCh38
NC_000006.11:g.132167921T>G , CM000668.1:g.132167921T>G GRCh37
NC_000006.10:g.132209614T>G NCBI36
NG_008206.1:g.43766T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000684147.1:n.519-995T>G
ENST00000647893.1:c.241-995T>G MANE Select ENSP00000498074.1:n.241-995T>G
ENST00000650507.1:c.248-995T>G ENSP00000497375.1:n.248-995T>G
ENST00000360971.6:c.241-995T>G ENSP00000354238.2:n.241-995T>G
ENST00000486853.1:n.261-995T>G
ENST00000513998.5:c.241-995T>G ENSP00000422424.1:n.241-995T>G
NM_006208.2:c.241-995T>G NP_006199.2:n.241-995T>G
NM_006208.3:c.241-995T>G MANE Select NP_006199.2:n.241-995T>G