Canonical Allele Identifier: CA147922479
Gene: ENPP1 HGNC NCBI

Identifiers and link-outs to other resources

dbSNP Id: rs997509

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131846837C>T , CM000668.2:g.131846837C>T GRCh38
NC_000006.11:g.132167977C>T , CM000668.1:g.132167977C>T GRCh37
NC_000006.10:g.132209670C>T NCBI36
NG_008206.1:g.43822C>T

Transcript Alleles

HGVS Amino-acid change
NM_006208.2:c.241-939C>T VV NP_006199.2:p.=
NM_006208.3:c.241-939C>T VV MANE Preferred NP_006199.2:p.=
ENST00000360971.6:c.241-939C>T ENSP00000354238.2:p.=
ENST00000486853.1:n.261-939C>T
ENST00000513998.5:c.241-939C>T ENSP00000422424.1:p.=