Canonical Allele Identifier: CA1664251962
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131846930A= , CM000668.2:g.131846930A= GRCh38
NC_000006.11:g.132168070A= , CM000668.1:g.132168070A= GRCh37
NC_000006.10:g.132209763A= NCBI36
NG_008206.1:g.43915A=

Transcript Alleles

HGVS Amino-acid change
ENST00000684147.1:n.519-846A=
ENST00000647893.1:c.241-846A= MANE Select ENSP00000498074.1:n.241-846A=
ENST00000650507.1:c.248-846A= ENSP00000497375.1:n.248-846A=
ENST00000360971.6:c.241-846A= ENSP00000354238.2:n.241-846A=
ENST00000486853.1:n.261-846A=
ENST00000513998.5:c.241-846A= ENSP00000422424.1:n.241-846A=
NM_006208.2:c.241-846A= NP_006199.2:n.241-846A=
NM_006208.3:c.241-846A= MANE Select NP_006199.2:n.241-846A=