Canonical Allele Identifier: CA2713036299
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs2114687699

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131846777G>A , CM000668.2:g.131846777G>A GRCh38
NC_000006.11:g.132167917G>A , CM000668.1:g.132167917G>A GRCh37
NC_000006.10:g.132209610G>A NCBI36
NG_008206.1:g.43762G>A

Transcript Alleles

HGVS Amino-acid change
ENST00000684147.1:n.519-999G>A
ENST00000647893.1:c.241-999G>A MANE Select ENSP00000498074.1:n.241-999G>A
ENST00000650507.1:c.248-999G>A ENSP00000497375.1:n.248-999G>A
ENST00000360971.6:c.241-999G>A ENSP00000354238.2:n.241-999G>A
ENST00000486853.1:n.261-999G>A
ENST00000513998.5:c.241-999G>A ENSP00000422424.1:n.241-999G>A
NM_006208.2:c.241-999G>A NP_006199.2:n.241-999G>A
NM_006208.3:c.241-999G>A MANE Select NP_006199.2:n.241-999G>A