Canonical Allele Identifier: CA1664283204
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1562188331

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890590C>G , CM000668.2:g.131890590C>G GRCh38
NC_000006.11:g.132211730C>G , CM000668.1:g.132211730C>G GRCh37
NC_000006.10:g.132253423C>G NCBI36
NG_008206.1:g.87575C>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684674.1:n.1288C>G
ENST00000647893.1:c.*79C>G MANE Select ENSP00000498074.1:n.*79C>G
ENST00000360971.6:c.*79C>G ENSP00000354238.2:n.*79C>G
ENST00000513998.5:c.*1694C>G ENSP00000422424.1:n.*1694C>G
NM_006208.2:c.*79C>G NP_006199.2:n.*79C>G
XM_011535896.1:c.*79C>G XP_011534198.1:n.*79C>G
NM_006208.3:c.*79C>G MANE Select NP_006199.2:n.*79C>G