Canonical Allele Identifier: CA1664283174
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1782455247

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890521dup , CM000668.2:g.131890521dup GRCh38
NC_000006.11:g.132211661dup , CM000668.1:g.132211661dup GRCh37
NC_000006.10:g.132253354dup NCBI36
NG_008206.1:g.87506dup

Transcript Alleles

HGVS Amino-acid Change
ENST00000684674.1:n.1219dup
ENST00000647893.1:c.*10dup MANE Select ENSP00000498074.1:n.*10dup
ENST00000360971.6:c.*10dup ENSP00000354238.2:n.*10dup
ENST00000513998.5:c.*1625dup ENSP00000422424.1:n.*1625dup
NM_006208.2:c.*10dup NP_006199.2:n.*10dup
XM_011535896.1:c.*10dup XP_011534198.1:n.*10dup
NM_006208.3:c.*10dup MANE Select NP_006199.2:n.*10dup