Canonical Allele Identifier: CA1664253803
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131851332_131851333delinsAG , CM000668.2:g.131851332_131851333delinsAG GRCh38
NC_000006.11:g.132172472_132172473delinsAG , CM000668.1:g.132172472_132172473delinsAG GRCh37
NC_000006.10:g.132214165_132214166delinsAG NCBI36
NG_008206.1:g.48317_48318delinsAG

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.556+65_556+66delinsAG MANE Select ENSP00000498074.1:n.556+65_556+66delinsAG
ENST00000650147.1:c.234+65_234+66delinsAG
ENST00000650437.1:c.108+1226_108+1227delinsAG
ENST00000360971.6:c.556+65_556+66delinsAG ENSP00000354238.2:n.556+65_556+66delinsAG
ENST00000486853.1:n.641_642delinsAG
ENST00000513998.5:c.556+65_556+66delinsAG ENSP00000422424.1:n.556+65_556+66delinsAG
NM_006208.2:c.556+65_556+66delinsAG NP_006199.2:n.556+65_556+66delinsAG
NM_006208.3:c.556+65_556+66delinsAG MANE Select NP_006199.2:n.556+65_556+66delinsAG