Canonical Allele Identifier: CA1664283176
Gene: ENPP1 HGNC NCBI

Genomic Alleles

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

Transcript Alleles

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