Canonical Allele Identifier: CA1664251882
Gene: ENPP1 HGNC NCBI

Genomic Alleles

HGVS Genome Assembly
NC_000006.12:g.131846750_131846751delinsAG , CM000668.2:g.131846750_131846751delinsAG GRCh38
NC_000006.11:g.132167890_132167891delinsAG , CM000668.1:g.132167890_132167891delinsAG GRCh37
NC_000006.10:g.132209583_132209584delinsAG NCBI36
NG_008206.1:g.43735_43736delinsAG

Transcript Alleles

HGVS Amino-acid change
ENST00000684147.1:n.519-1026_519-1025delinsAG
ENST00000647893.1:c.241-1026_241-1025delinsAG MANE Select ENSP00000498074.1:n.241-1026_241-1025deli...
ENST00000650507.1:c.248-1026_248-1025delinsAG ENSP00000497375.1:n.248-1026_248-1025deli...
ENST00000360971.6:c.241-1026_241-1025delinsAG ENSP00000354238.2:n.241-1026_241-1025deli...
ENST00000486853.1:n.261-1026_261-1025delinsAG
ENST00000513998.5:c.241-1026_241-1025delinsAG ENSP00000422424.1:n.241-1026_241-1025deli...
NM_006208.2:c.241-1026_241-1025delinsAG NP_006199.2:n.241-1026_241-1025delinsAG
NM_006208.3:c.241-1026_241-1025delinsAG MANE Select NP_006199.2:n.241-1026_241-1025delinsAG