Canonical Allele Identifier: CA1664253889
Gene: ENPP1 HGNC NCBI
JSON-LD

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131851552C= , CM000668.2:g.131851552C= GRCh38
NC_000006.11:g.132172692C= , CM000668.1:g.132172692C= GRCh37
NC_000006.10:g.132214385C= NCBI36
NG_008206.1:g.48537C=

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.556+285C= MANE Select ENSP00000498074.1:n.556+285C=
ENST00000650147.1:c.234+285C=
ENST00000650437.1:c.108+1446C=
ENST00000360971.6:c.556+285C= ENSP00000354238.2:n.556+285C=
ENST00000513998.5:c.556+285C= ENSP00000422424.1:n.556+285C=
NM_006208.2:c.556+285C= NP_006199.2:n.556+285C=
NM_006208.3:c.556+285C= MANE Select NP_006199.2:n.556+285C=
Search 100 bp 5'
Search 100 bp 3'