Canonical Allele Identifier: CA2713036019

Gene: ENPP1

Linked Data

• dbSNP Id: rs2114672538

Genomic Alleles

HGVS	Genome Assembly
NC_000006.12:g.131832669C>G , CM000668.2:g.131832669C>G	GRCh38
NC_000006.11:g.132153809C>G , CM000668.1:g.132153809C>G	GRCh37
NC_000006.10:g.132195502C>G	NCBI36
NG_008206.1:g.29654C>G

Transcript Alleles

HGVS	Amino-acid change
ENST00000647893.1:c.241-15107C>G MANE Select	ENSP00000498074.1:n.241-15107C>G
ENST00000650507.1:c.247+6554C>G	ENSP00000497375.1:n.247+6554C>G
ENST00000360971.6:c.241-15107C>G	ENSP00000354238.2:n.241-15107C>G
ENST00000486853.1:n.261-15107C>G
ENST00000513998.5:c.241-15107C>G	ENSP00000422424.1:n.241-15107C>G
NM_006208.2:c.241-15107C>G	NP_006199.2:n.241-15107C>G
NM_006208.3:c.241-15107C>G MANE Select	NP_006199.2:n.241-15107C>G