Canonical Allele Identifier: CA1664253724
Gene: ENPP1 HGNC NCBI

Linked Data

dbSNP Id: rs1781875359

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131851149_131851150del , CM000668.2:g.131851149_131851150del GRCh38
NC_000006.11:g.132172289_132172290del , CM000668.1:g.132172289_132172290del GRCh37
NC_000006.10:g.132213982_132213983del NCBI36
NG_008206.1:g.48134_48135del

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.438_439del MANE Select ENSP00000498074.1:p.Ile146MetfsTer10
ENST00000650147.1:c.116_117del
ENST00000650437.1:c.108+1043_108+1044del
ENST00000360971.6:c.438_439del ENSP00000354238.2:p.Ile146MetfsTer10
ENST00000486853.1:n.458_459del
ENST00000513998.5:c.438_439del ENSP00000422424.1:p.Ile146MetfsTer10
NM_006208.2:c.438_439del NP_006199.2:p.Ile146MetfsTer10
NM_006208.3:c.438_439del MANE Select NP_006199.2:p.Ile146MetfsTer10