Canonical Allele Identifier: CA1664253759
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131851241G= , CM000668.2:g.131851241G= GRCh38
NC_000006.11:g.132172381G= , CM000668.1:g.132172381G= GRCh37
NC_000006.10:g.132214074G= NCBI36
NG_008206.1:g.48226G=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.530G= MANE Select ENSP00000498074.1:p.Cys177=
ENST00000650147.1:c.208G=
ENST00000650437.1:c.108+1135G=
ENST00000360971.6:c.530G= ENSP00000354238.2:p.Cys177=
ENST00000486853.1:n.550G=
ENST00000513998.5:c.530G= ENSP00000422424.1:p.Cys177=
NM_006208.2:c.530G= NP_006199.2:p.Cys177=
NM_006208.3:c.530G= MANE Select NP_006199.2:p.Cys177=