Canonical Allele Identifier: CA1664283186
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131890534C= , CM000668.2:g.131890534C= GRCh38
NC_000006.11:g.132211674C= , CM000668.1:g.132211674C= GRCh37
NC_000006.10:g.132253367C= NCBI36
NG_008206.1:g.87519C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000684674.1:n.1232C=
ENST00000647893.1:c.*23C= MANE Select ENSP00000498074.1:n.*23C=
ENST00000360971.6:c.*23C= ENSP00000354238.2:n.*23C=
ENST00000513998.5:c.*1638C= ENSP00000422424.1:n.*1638C=
NM_006208.2:c.*23C= NP_006199.2:n.*23C=
XM_011535896.1:c.*23C= XP_011534198.1:n.*23C=
NM_006208.3:c.*23C= MANE Select NP_006199.2:n.*23C=