Canonical Allele Identifier: CA1664251889
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131846764C= , CM000668.2:g.131846764C= GRCh38
NC_000006.11:g.132167904C= , CM000668.1:g.132167904C= GRCh37
NC_000006.10:g.132209597C= NCBI36
NG_008206.1:g.43749C=

Transcript Alleles

HGVS Amino-acid change
ENST00000684147.1:n.519-1012C=
ENST00000647893.1:c.241-1012C= MANE Select ENSP00000498074.1:n.241-1012C=
ENST00000650507.1:c.248-1012C= ENSP00000497375.1:n.248-1012C=
ENST00000360971.6:c.241-1012C= ENSP00000354238.2:n.241-1012C=
ENST00000486853.1:n.261-1012C=
ENST00000513998.5:c.241-1012C= ENSP00000422424.1:n.241-1012C=
NM_006208.2:c.241-1012C= NP_006199.2:n.241-1012C=
NM_006208.3:c.241-1012C= MANE Select NP_006199.2:n.241-1012C=