Canonical Allele Identifier: CA1664283144
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890450A= , CM000668.2:g.131890450A= GRCh38
NC_000006.11:g.132211590A= , CM000668.1:g.132211590A= GRCh37
NC_000006.10:g.132253283A= NCBI36
NG_008206.1:g.87435A=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684674.1:n.1148A=
ENST00000647893.1:c.2717A= MANE Select ENSP00000498074.1:p.Glu906=
ENST00000360971.6:c.2717A= ENSP00000354238.2:p.Glu906=
ENST00000513998.5:c.*1554A= ENSP00000422424.1:n.*1554A=
NM_006208.2:c.2717A= NP_006199.2:p.Glu906=
XM_011535896.1:c.1607A= XP_011534198.1:p.Glu536=
NM_006208.3:c.2717A= MANE Select NP_006199.2:p.Glu906=