Canonical Allele Identifier: CA1664260164
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131861621C= , CM000668.2:g.131861621C= GRCh38
NC_000006.11:g.132182761C= , CM000668.1:g.132182761C= GRCh37
NC_000006.10:g.132224454C= NCBI36
NG_008206.1:g.58606C=

Transcript Alleles

HGVS Amino-acid change
ENST00000647893.1:c.942C= MANE Select ENSP00000498074.1:p.Gly314=
ENST00000650147.1:c.559C=
ENST00000650437.1:c.433C=
ENST00000360971.6:c.942C= ENSP00000354238.2:p.Gly314=
ENST00000459624.1:n.12C=
ENST00000513998.5:c.942C= ENSP00000422424.1:p.Gly314=
NM_006208.2:c.942C= NP_006199.2:p.Gly314=
NM_006208.3:c.942C= MANE Select NP_006199.2:p.Gly314=