Canonical Allele Identifier: CA1664283170
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs769637866

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890513A>G , CM000668.2:g.131890513A>G GRCh38
NC_000006.11:g.132211653A>G , CM000668.1:g.132211653A>G GRCh37
NC_000006.10:g.132253346A>G NCBI36
NG_008206.1:g.87498A>G

Transcript Alleles

HGVS Amino-acid Change
ENST00000684674.1:n.1211A>G
ENST00000647893.1:c.*2A>G MANE Select ENSP00000498074.1:n.*2A>G
ENST00000360971.6:c.*2A>G ENSP00000354238.2:n.*2A>G
ENST00000513998.5:c.*1617A>G ENSP00000422424.1:n.*1617A>G
NM_006208.2:c.*2A>G NP_006199.2:n.*2A>G
XM_011535896.1:c.*2A>G XP_011534198.1:n.*2A>G
NM_006208.3:c.*2A>G MANE Select NP_006199.2:n.*2A>G