Canonical Allele Identifier: CA1664240926
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131832848_131832862delinsTACATGGAGGCTGAA , CM000668.2:g.131832848_131832862delinsTACATGGAGGCTGAA GRCh38
NC_000006.11:g.132153988_132154002delinsTACATGGAGGCTGAA , CM000668.1:g.132153988_132154002delinsTACATGGAGGCTGAA GRCh37
NC_000006.10:g.132195681_132195695delinsTACATGGAGGCTGAA NCBI36
NG_008206.1:g.29833_29847delinsTACATGGAGGCTGAA

Transcript Alleles

HGVS Amino-acid Change
ENST00000647893.1:c.241-14928_241-14914delinsTACATGGAGGCTGAA MANE Select ENSP00000498074.1:n.241-14928_241-14914delinsTACATGGAGGCTGAA
ENST00000650507.1:c.247+6733_247+6747delinsTACATGGAGGCTGAA ENSP00000497375.1:n.247+6733_247+6747delinsTACATGGAGGCTGAA
ENST00000360971.6:c.241-14928_241-14914delinsTACATGGAGGCTGAA ENSP00000354238.2:n.241-14928_241-14914delinsTACATGGAGGCTGAA
ENST00000486853.1:n.261-14928_261-14914delinsTACATGGAGGCTGAA
ENST00000513998.5:c.241-14928_241-14914delinsTACATGGAGGCTGAA ENSP00000422424.1:n.241-14928_241-14914delinsTACATGGAGGCTGAA
NM_006208.2:c.241-14928_241-14914delinsTACATGGAGGCTGAA NP_006199.2:n.241-14928_241-14914delinsTACATGGAGGCTGAA
NM_006208.3:c.241-14928_241-14914delinsTACATGGAGGCTGAA MANE Select NP_006199.2:n.241-14928_241-14914delinsTACATGGAGGCTGAA