Canonical Allele Identifier: CA1664257152
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1781979653

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131858656T>G , CM000668.2:g.131858656T>G GRCh38
NC_000006.11:g.132179796T>G , CM000668.1:g.132179796T>G GRCh37
NC_000006.10:g.132221489T>G NCBI36
NG_008206.1:g.55641T>G

Transcript Alleles

HGVS Amino-acid change
ENST00000647893.1:c.716-12T>G MANE Select ENSP00000498074.1:n.716-12T>G
ENST00000650147.1:c.333-12T>G
ENST00000650437.1:c.207-12T>G
ENST00000360971.6:c.716-12T>G ENSP00000354238.2:n.716-12T>G
ENST00000513998.5:c.716-12T>G ENSP00000422424.1:n.716-12T>G
NM_006208.2:c.716-12T>G NP_006199.2:n.716-12T>G
NM_006208.3:c.716-12T>G MANE Select NP_006199.2:n.716-12T>G