Canonical Allele Identifier: CA1664283166
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1782454905

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890510_131890512dup , CM000668.2:g.131890510_131890512dup GRCh38
NC_000006.11:g.132211650_132211652dup , CM000668.1:g.132211650_132211652dup GRCh37
NC_000006.10:g.132253343_132253345dup NCBI36
NG_008206.1:g.87495_87497dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000684674.1:n.1208_1210dup
ENST00000647893.1:c.2777_*1dup MANE Select ENSP00000498074.1:n.2777_*1dup
ENST00000360971.6:c.2777_*1dup ENSP00000354238.2:n.2777_*1dup
ENST00000513998.5:c.*1614_*1616dup ENSP00000422424.1:n.*1614_*1616dup
NM_006208.2:c.2777_*1dup NP_006199.2:n.2777_*1dup
XM_011535896.1:c.1667_*1dup XP_011534198.1:n.1667_*1dup
NM_006208.3:c.2777_*1dup MANE Select NP_006199.2:n.2777_*1dup