Canonical Allele Identifier: CA2773093491
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131851395_131851396insA , CM000668.2:g.131851395_131851396insA GRCh38
NC_000006.11:g.132172535_132172536insA , CM000668.1:g.132172535_132172536insA GRCh37
NC_000006.10:g.132214228_132214229insA NCBI36
NG_008206.1:g.48380_48381insA

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.556+128_556+129insA MANE Select ENSP00000498074.1:n.556+128_556+129insA
ENST00000650147.1:c.234+128_234+129insA
ENST00000650437.1:c.108+1289_108+1290insA
ENST00000360971.6:c.556+128_556+129insA ENSP00000354238.2:n.556+128_556+129insA
ENST00000486853.1:n.704_705insA
ENST00000513998.5:c.556+128_556+129insA ENSP00000422424.1:n.556+128_556+129insA
NM_006208.2:c.556+128_556+129insA NP_006199.2:n.556+128_556+129insA
NM_006208.3:c.556+128_556+129insA MANE Select NP_006199.2:n.556+128_556+129insA