Canonical Allele Identifier: CA1664251902
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1781816914

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131846803dup , CM000668.2:g.131846803dup GRCh38
NC_000006.11:g.132167943dup , CM000668.1:g.132167943dup GRCh37
NC_000006.10:g.132209636dup NCBI36
NG_008206.1:g.43788dup

Transcript Alleles

HGVS Amino-acid change
ENST00000684147.1:n.519-973dup
ENST00000647893.1:c.241-973dup MANE Select ENSP00000498074.1:n.241-973dup
ENST00000650507.1:c.248-973dup ENSP00000497375.1:n.248-973dup
ENST00000360971.6:c.241-973dup ENSP00000354238.2:n.241-973dup
ENST00000486853.1:n.261-973dup
ENST00000513998.5:c.241-973dup ENSP00000422424.1:n.241-973dup
NM_006208.2:c.241-973dup NP_006199.2:n.241-973dup
NM_006208.3:c.241-973dup MANE Select NP_006199.2:n.241-973dup