Canonical Allele Identifier: CA1664283219
Gene: ENPP1 HGNC NCBI
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Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890618A= , CM000668.2:g.131890618A= GRCh38
NC_000006.11:g.132211758A= , CM000668.1:g.132211758A= GRCh37
NC_000006.10:g.132253451A= NCBI36
NG_008206.1:g.87603A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684674.1:n.1316A=
ENST00000647893.1:c.*107A= MANE Select ENSP00000498074.1:n.*107A=
ENST00000360971.6:c.*107A= ENSP00000354238.2:n.*107A=
ENST00000513998.5:c.*1722A= ENSP00000422424.1:n.*1722A=
NM_006208.2:c.*107A= NP_006199.2:n.*107A=
XM_011535896.1:c.*107A= XP_011534198.1:n.*107A=
NM_006208.3:c.*107A= MANE Select NP_006199.2:n.*107A=
Search 100 bp 5'
Search 100 bp 3'